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).

摘要第一期素失禁症典型皮肤临床表现是一整排水泡加上基底。

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

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

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岁男性病患，在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).

摘要第一期色症典型皮肤临床表现是一整排水泡加上红色基底。

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

色症是一种罕见皮肤遗传疾病，通常发生在女，除了皮肤以外还能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

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岁病患，在使用抗凝血剂之后数小时引起急下背痛，且合并有及下肢无力症状。

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典型皮肤临床表现是一整排水泡加上红色基底。

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.

出一位29岁男性病患，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，除了皮肤外还能出现眼睛，牙齿，骨骼，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，除了皮肤外还能出现眼睛，牙齿，骨骼，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.

色素失禁症是一种罕见的皮肤遗传疾病，通常发生在女，皮肤以外还能出现眼睛，，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岁的男病患，在使用抗凝血剂之后数小时引起急下背痛，且合并有失禁及下肢无力的症状。