Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一期色素失禁症的典型临床表现是一整排的水泡加上红色的基底。

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遗传疾病，通常发生在女性，除以外还能出现，齿，骨骼，以及中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性下背痛，且合并有失禁及下肢无力的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一期色素失禁症的典型床表现是一整排的水泡加上红色的基底。

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遗传疾病，通常发生在女性，除了以外还能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性，且合并有失禁及肢无力的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一失禁症的典型皮肤临床表现是一整排的水泡加上红的基底。

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

失禁症是一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还能出现眼睛，牙齿，骨骼，以中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性背痛，且合并有失禁无力的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要色素失禁症的典型皮肤临床表现是整排的水泡加上红色的基底。

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

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

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出位29岁的男性病患，在使用抗凝血剂之后数小时引起急性下背痛，且合并有失禁及下的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第期色素失禁症的典型皮肤临床表现整排的水泡加上红色的基底。

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

色素失禁症罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还能现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提29岁的男性病患，在使用抗凝血剂之后数小时引起急性下背痛，且合并有失禁及下肢无力的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一期色素失禁症的典型皮肤临床表现是一整排的水泡加红色的基底。

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，通常发生在女性，除了皮肤以外还能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性下背痛，且合并有失禁及下肢无力的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一期色素失禁症的典型临床表现是一整排的水泡加上红色的基底。

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遗传疾病，通常发生在女性，除以外还能出现，齿，骨骼，以及中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性下背痛，且合并有失禁及下肢无力的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一失禁症的典型皮肤临床表现是一整排的水泡加上红的基底。

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

失禁症是一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还能出现眼睛，牙齿，骨骼，以中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性背痛，且合并有失禁无力的症状。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

要第一期色素失禁的典型皮肤临床表现是一整排的水泡加上红色的基底。

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，除了皮肤以外还能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性下背痛，且合并有失禁及下肢无力的。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一期色素失禁症的典型床表现是一整排的水泡加上红色的基底。

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遗传疾病，通常发生在女性，除了以外还能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

We present a 29 year-old male with a history of coumadin therapy for deep vein thrombosis who developed exsanguinating lower back pain and progressive neurological deterioration.

我们提出一位29岁的男性病患，在使用抗凝血剂之后数小时引起急性，且合并有失禁及肢无力的症状。