Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)具有皮脂腺分化特徵的罕见表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种罕见的麻痹症从他的踝部扩散开来，最终道致他的。

It was a time when motorcars were rare.

汽车很罕见的时代。

The unusually hot sun has fried up the crops.

罕见的烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场罕见的洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形外科医生诊断出我的病一种罕见的骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我的病为罕见的皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种罕见的癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要先天性自愈性网状组织细胞增生症兰格罕氏组织细胞增生症中罕见的一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种罕见的先天性疾病“并腿畸形”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激素释放因子治疗相关的副作见的，但严重到足以停药的程度罕见的。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕见的上皮性和非上皮性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症一种罕见的皮肤遗传疾病，通发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出种罕见的先天性异，其成因为头颅或眼窝骨的缺损使得脑脑从缺损处呈囊状的膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽'海伊井综合徵-罕见的先天性条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，一种罕见的中耳腔血管异。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中的集聚，我们报告一例罕见的系统性肥大症与胆汁淤积性肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症相当罕见的一种先天性脚趾（手指）过度增生的一种畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见的遗传性掌跖皮肤角化病—遗传性毁性角化瘤,并与各种掌跖皮肤角化症、断肢症的鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)是具有皮脂腺分化特徵表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种麻痹症从他踝部扩散开来，最终道致他残废。

It was a time when motorcars were rare.

那是汽车很时代。

The unusually hot sun has fried up the crops.

烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形生诊断出我病是一种骨病。

The doctor diagnosed my illness as a rare skin disease.

生诊断我病为皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要先天性自愈性网状组织细胞增生症是兰格氏组织细胞增生症中一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种先天性疾病“并腿畸形”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激素释放因子治疗相关副作用是常，但严重到足以停药程度是。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例上皮性和非上皮性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种皮肤遗传疾病，通常发生在女性，除了皮肤以还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出是种先天性异常，其成因为头颅或眼窝骨缺损使得脑脑从缺损处呈囊状膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-先天性条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种代谢功能紊乱疾病，因为缺乏分解半乳糖酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一种中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中集聚，我们报告一例系统性肥大症与胆汁淤积性肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症是相当一种先天性脚趾（手指）过度增生一种畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例遗传性掌跖皮肤角化病—遗传性残毁性角化瘤,并与各种掌跖皮肤角化症、断肢症鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)是具有皮脂腺分化特徵罕表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种罕麻痹症从他踝部扩散开来，最终道致他残废。

It was a time when motorcars were rare.

那是汽车很罕时代。

The unusually hot sun has fried up the crops.

罕烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨因为一场罕洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形外科医生诊断出我病是一种罕骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我病为罕皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种罕症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要自愈网状组织细胞增生症是兰格罕氏组织细胞增生症中罕一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种罕疾病“并腿畸形”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促腺激素释放因子治疗相关副作用是常，但严重到足以停药程度是罕。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕上皮和非上皮泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕皮肤遗传疾病，通常发生在女，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出是种罕异常，其成因为头颅或眼窝骨缺损使得脑脑从缺损处呈囊状膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-罕条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕代谢功能紊乱疾病，因为缺乏分解半乳糖酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一种罕中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统肥大导致肥大细胞在各组织中集聚，我们报告一例罕系统肥大症与胆汁淤积肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症是相当罕一种脚趾（手指）过度增生一种畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕遗传掌跖皮肤角化病—遗传残毁角化瘤,并与各种掌跖皮肤角化症、断肢症鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)是具有皮脂腺分化特徵罕表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一罕麻痹症从他踝部扩散开来，最终道致他残废。

It was a time when motorcars were rare.

那是汽车很罕时代。

The unusually hot sun has fried up the crops.

罕烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场罕水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整外科医生诊断出我病是一罕骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我病为罕皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某罕癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要先天性自愈性网状组织细胞增生症是兰格罕氏组织细胞增生症中罕一型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一罕先天性疾病“并腿畸”，病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激素释放因子治疗相关副作用是常，但严重到足以停药程度是罕。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕上皮性和非上皮性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一罕皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出是罕先天性异常，其成因为头颅或眼窝骨缺损使得脑脑从缺损处呈囊状膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-罕先天性条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一罕代谢功能紊乱疾病，因为缺乏分解半乳糖酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一罕中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中集聚，我们报告一例罕系统性肥大症与胆汁淤积性肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症是相当罕一先天性脚趾（手指）过度增生一畸，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕遗传性掌跖皮肤角化病—遗传性残毁性角化瘤,并与各掌跖皮肤角化症、断肢症鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)是具有皮脂腺分化特徵的罕见表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种罕见的麻痹症从他的踝部扩散开来，最终道致他的残废。

It was a time when motorcars were rare.

那是汽车很罕见的时代。

The unusually hot sun has fried up the crops.

罕见的烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场罕见的洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形外科医生诊断出我的病是一种罕见的骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我的病为罕见的皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种罕见的癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要先天自愈网状组织细胞增生症是兰格罕氏组织细胞增生症中罕见的一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种罕见的先天疾病“并腿畸形”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促腺激素释放因子治疗相关的副作用是常见的，但严重到足以停药的程度是罕见的。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕见的上皮和非上皮泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通常发生，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出是种罕见的先天异常，其成因为头颅或眼窝骨的缺损使得脑脑从缺损处呈囊状的膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-罕见的先天条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一种罕见的中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统肥大导致肥大细胞各组织中的集聚，我们报告一例罕见的系统肥大症与胆汁淤积肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症是相当罕见的一种先天脚趾（手指）过度增生的一种畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见的遗传掌跖皮肤角化病—遗传残毁角化瘤,并与各种掌跖皮肤角化症、断肢症的鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

皮脂瘤(皮脂腺上皮瘤)是具有皮脂腺分化特徵的罕见表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种罕见的麻痹从他的踝部扩散开来，最终道致他的残废。

It was a time when motorcars were rare.

那是汽车很罕见的时代。

The unusually hot sun has fried up the crops.

罕见的烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场罕见的洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形外科医生诊断出我的病是一种罕见的骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我的病为罕见的皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种罕见的。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

天性自愈性网状组织细胞增生是兰格罕氏组织细胞增生中罕见的一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种罕见的天性疾病“并腿畸形”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激素释放因子治疗相关的副作用是常见的，但严重到足以停药的程度是罕见的。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕见的上皮性和非上皮性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁是一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

眼窝脑膜膨出是种罕见的天性异常，其成因为头颅或眼窝骨的缺损使得脑脑从缺损处呈囊状的膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-罕见的天性条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血是另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一种罕见的中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中的集聚，我们报告一例罕见的系统性肥大与胆汁淤积性肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

巨趾（指）是相当罕见的一种天性脚趾（手指）过度增生的一种畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见的遗传性掌跖皮肤角化病—遗传性残毁性角化瘤,并与各种掌跖皮肤角化、断肢的鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)具有皮脂腺分化特徵的罕见表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种罕见的麻痹症从他的踝部扩散开来，最终道致他的残。

It was a time when motorcars were rare.

汽车很罕见的时代。

The unusually hot sun has fried up the crops.

罕见的烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场罕见的洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形外科医生诊断出我的病一种罕见的骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我的病为罕见的皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种罕见的癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要先天性自愈性网状组织细胞增生症兰格罕氏组织细胞增生症中罕见的一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种罕见的先天性疾病“并腿畸形”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激素释放因子治疗相关的副常见的，但严重到足以停药的程度罕见的。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕见的上皮性和非上皮性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出种罕见的先天性异常，其成因为头颅或眼窝骨的缺损使得脑脑从缺损处呈囊状的膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽'海伊井综合徵-罕见的先天性条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，一种罕见的中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中的集聚，我们报告一例罕见的系统性肥大症与胆汁淤积性肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症相当罕见的一种先天性脚趾（手指）过度增生的一种畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见的遗传性掌跖皮肤角化病—遗传性残毁性角化瘤,并与各种掌跖皮肤角化症、断肢症的鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)是具有皮脂腺分化特徵罕见表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种罕见麻痹症从他踝部扩散开来，最终道致他残废。

It was a time when motorcars were rare.

那是汽车很罕见时代。

The unusually hot sun has fried up the crops.

罕见烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨因为一场罕见洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

科医生诊断出我病是一种罕见骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我病为罕见皮肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种罕见癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要性自愈性网状组织细胞增生症是兰格罕氏组织细胞增生症中罕见一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种罕见性疾病“并腿畸”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激素释放因子治疗相关副作用是常见，但严重到足以停药程度是罕见。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕见上皮性和非上皮性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤遗传疾病，通常发生在女性，除了皮肤以还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出是种罕见性异常，其成因为头颅或眼窝骨缺损使得脑脑从缺损处呈囊状膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-罕见性条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见代谢功能紊乱疾病，因为缺乏分解半乳糖酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一种罕见中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中集聚，我们报告一例罕见系统性肥大症与胆汁淤积性肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症是相当罕见一种性脚趾（手指）过度增生一种畸，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见遗传性掌跖皮肤角化病—遗传性残毁性角化瘤,并与各种掌跖皮肤角化症、断肢症鉴别进行了讨论。

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要瘤(腺上瘤)是具有腺分化特徵的罕见表附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一种罕见的麻痹症从他的踝部扩散开来，最终道致他的残废。

It was a time when motorcars were rare.

那是汽车很罕见的时代。

The unusually hot sun has fried up the crops.

罕见的烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场罕见的洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形外科医生诊断出我的病是一种罕见的骨病。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我的病为罕见的肤病。

Aids victims often develop a rare type of cancer.

艾滋病患者往往会罹患某种罕见的癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要先天性自愈性网状组织细胞增生症是兰格罕氏组织细胞增生症中罕见的一种型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一种罕见的先天性疾病“并腿畸形”，这种病又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激释放因子治疗相关的副作用是常见的，但严重到足以停药的程度是罕见的。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例罕见的上性和非上性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

禁症是一种罕见的肤遗传疾病，通常发生在女性，除了肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出是种罕见的先天性异常，其成因为头颅或眼窝骨的缺损使得脑脑从缺损处呈囊状的膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-罕见的先天性条件影响肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一种罕见的中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中的集聚，我们报告一例罕见的系统性肥大症与胆汁淤积性肝病。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症是相当罕见的一种先天性脚趾（手指）过度增生的一种畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见的遗传性掌跖肤角化病—遗传性残毁性角化瘤,并与各种掌跖肤角化症、断肢症的鉴别进行了讨论。