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Herditary Anhidrotic Ectodermal Dysplasia in Twins
Journal of the Korean Pediatric Society ; : 1005-1009, 1996.
Article in Korean | WPRIM | ID: wpr-193834
ABSTRACT
Hereditary anhidrotic ectodermal Dysplasia is a congenital disease displaying characteristics of anhidrosis, hypotrichosis and dental defect which are caused by developmental anomaly of ectodermal epidermis and its appendages. We experienced two cases of hereditary anhidrotic ectodermal dysplasia in two-year and four-month old twin brothers. These patients suffered from intermittent high fever early in life which brought them to our clinical attention. However the diagnosis of anhidrotic ectodermal dysplasia was not suspected by means physicians who cared the patients previously. The diagnosis was made on the basis of clinical features, and confirmed by starch iodine sweat test and skin biopsy on the palm and axilla. We report the two cases in a twin brothers with brief review of related literatures.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Starch / Axilla / Sweat / Twins / Biopsy / Ectodermal Dysplasia / Siblings / Diagnosis / Ectoderm Type of study: Diagnostic study Limits: Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 1996 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Starch / Axilla / Sweat / Twins / Biopsy / Ectodermal Dysplasia / Siblings / Diagnosis / Ectoderm Type of study: Diagnostic study Limits: Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 1996 Type: Article