[Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy].
Hautarzt. 1987 Sep; 38(9):532-5.H

Abstract

A family suffering from hypotrichosis congenita hereditaria Marie Unna is reported (16 members affected in five generations). The typical symptoms of this autosomal dominant syndrome were found: pili torti, canaliculi et trianguli, inborn generalized hypotrichosis, later on resulting in alopecia of the androgenetic type. A 19-year-old female patient with hyperandrogenemia was treated with cyproterone acetate and ethinyl estradiol. Furthermore, hypotrichosis was associated with Ehlers-Danlos syndrome and atopic symptoms in the last three generations of the family. There does not seem to be any genetic connection between the syndromes however.

Authors+Show Affiliations

Mende B

Hautklinik und Poliklinik, Rheinischen Friedrich-Wilhelms-Universität Bonn.

Kreysel HW

No affiliation info available

MeSH

AdultAlopeciaDermatitis, AtopicEhlers-Danlos SyndromeFemaleHumansHypotrichosisPedigree

Pub Type(s)

Case Reports

English Abstract

Journal Article

Language

ger

PubMed ID

3692855

Citation

Mende, B, and H W. Kreysel. "[Hypotrichosis Congenita Hereditaria Marie Unna With Ehlers-Danlos Syndrome and Atopy]." Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, vol. 38, no. 9, 1987, pp. 532-5.

Mende B, Kreysel HW. [Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy]. Hautarzt. 1987;38(9):532-5.

Mende, B., & Kreysel, H. W. (1987). [Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy]. Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, 38(9), 532-5.

Mende B, Kreysel HW. [Hypotrichosis Congenita Hereditaria Marie Unna With Ehlers-Danlos Syndrome and Atopy]. Hautarzt. 1987;38(9):532-5. PubMed PMID: 3692855.

* Article titles in AMA citation format should be in sentence-case

TY - JOUR T1 - [Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy]. AU - Mende,B, AU - Kreysel,H W, PY - 1987/9/1/pubmed PY - 1987/9/1/medline PY - 1987/9/1/entrez SP - 532 EP - 5 JF - Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete JO - Hautarzt VL - 38 IS - 9 N2 - A family suffering from hypotrichosis congenita hereditaria Marie Unna is reported (16 members affected in five generations). The typical symptoms of this autosomal dominant syndrome were found: pili torti, canaliculi et trianguli, inborn generalized hypotrichosis, later on resulting in alopecia of the androgenetic type. A 19-year-old female patient with hyperandrogenemia was treated with cyproterone acetate and ethinyl estradiol. Furthermore, hypotrichosis was associated with Ehlers-Danlos syndrome and atopic symptoms in the last three generations of the family. There does not seem to be any genetic connection between the syndromes however. SN - 0017-8470 UR - https://wwww.unboundmedicine.com/medline/citation/3692855/[Hypotrichosis_congenita_hereditaria_Marie_Unna_with_Ehlers_Danlos_syndrome_and_atopy]_ DB - PRIME DP - Unbound Medicine ER -

Tags

[Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy].Hautarzt. 1987 Sep; 38(9):532-5.H