Hereditary hypotrichosis simplex of the scalp.
Dermatology
; 191(2): 139-41, 1995.
Article
em En
| MEDLINE
| ID: mdl-8520061
ABSTRACT
We report on a female aged 13 years, whose scalp hair began to disappear at the age of 9 years, leaving only sparse wispy hairs in the parietal-occipital region. Eyelashes, eyebrows and body hair were unaffected. There were no signs of ectodermal dysplasia on the skin, nails, teeth and eyes nor other congenital abnormalities. The family pedigree showed 15 relatives similarly affected according to an autosomal dominant mode of transmission. Clinical, genetic, histological and ultrastructural aspects led to a diagnosis of hereditary hypotrichosis simplex of the scalp (Toribio-Quiñones type).
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Base de dados:
MEDLINE
Assunto principal:
Hipotricose
Limite:
Adolescent
/
Female
/
Humans
Idioma:
En
Revista:
Dermatology
Assunto da revista:
DERMATOLOGIA
Ano de publicação:
1995
Tipo de documento:
Article
País de afiliação:
Espanha