A Rapp-Hodgkin like syndrome in three sibs: clinical, dental and dermatoglyphic study.
Clin Dysmorphol
; 8(2): 101-10, 1999 Apr.
Article
de En
| MEDLINE
| ID: mdl-10319198
ABSTRACT
Rapp-Hodgkin ectodermal dysplasia is an autosomal dominant disorder characterized by distinctive craniofacies, cleft lip or palate, oligodontia or anodontia, hypoplasia of the nails, and a decrease in or absence of the sweat glands and hair follicles. We have identified a family in which three children display clinical features similar to Rapp-Hodgkin syndrome. The father and two other sisters of the patient had normal facial features, but had short stature and had dental anomalies, the latter suggestive of ectodermal dysplasia. The overall clinical, dental, and dermatoglyphic findings of these patients are discussed in relation to reports of families with Rapp-Hodgkin syndrome.
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Collection:
01-internacional
Base de données:
MEDLINE
Sujet principal:
Malformations dentaires
/
Malformations multiples
/
Dysplasie ectodermique
/
Dermatoglyphes
Type d'étude:
Prognostic_studies
Limites:
Adolescent
/
Adult
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Langue:
En
Journal:
Clin Dysmorphol
Sujet du journal:
TERATOLOGIA
Année:
1999
Type de document:
Article
Pays d'affiliation:
Turquie