[Hair anomalies in syndromic disorders].
Haaranomalien bei syndromalen Erkrankungen.
Alopecia
Congenital abnormalities
Ectodermal dysplasia
Hypertrichosis
Hypotrichosis
Journal
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete
ISSN: 1432-1173
Titre abrégé: Hautarzt
Pays: Germany
ID NLM: 0372755
Informations de publication
Date de publication:
Jul 2019
Jul 2019
Historique:
pubmed:
15
6
2019
medline:
10
9
2019
entrez:
15
6
2019
Statut:
ppublish
Résumé
Genetic diseases with hyper- and hypotrichosis are very heterogeneous, both clinically and genetically. This is especially true for ectodermal dysplasias but also for hereditary syndromes in which, beyond abnormal hair growth, other structures and organs are affected. In this review, we discuss distinct diseases with excessive and reduced hair growth, focusing on the clinical hallmarks and underlying genetic defects.
Identifiants
pubmed: 31197391
doi: 10.1007/s00105-019-4440-6
pii: 10.1007/s00105-019-4440-6
doi:
Types de publication
Journal Article
Review
Langues
ger
Sous-ensembles de citation
IM
Pagination
514-519Références
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