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Journal of the Korean Pediatric Society ; : 1453-1456, 1994.
Article in Korean | WPRIM | ID: wpr-84938

ABSTRACT

Hereditary anhidrotic ectodermal dysplasia is a rare condition characterized by underdeveloped ectodermal structure including the skin, teeth or skin appendages. The patient has characteristic feature of anhidrosis, hypotrichosis and defective dentition. We experienced a case of hereditary anhidrotic ectodermal dysplasia in a l-month-old male infant who had unexplained recurring fever, anhidrosis and characteristic facial feature, so we established the diagnosis with clinical feature and skin biopsy.


Subject(s)
Humans , Infant , Male , Biopsy , Dentition , Diagnosis , Ectoderm , Ectodermal Dysplasia , Fever , Hypohidrosis , Hypotrichosis , Skin , Tooth
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