Hereditary hypotrichosis simplex

M. Just; M. Ribera; M. J. Fuente; I. Bielsa; Carlos Ferrándiz

doi:10.1159/000017909

Hereditary hypotrichosis simplex

M. Just, M. Ribera, M. J. Fuente, I. Bielsa, Carlos Ferrándiz

Departament de Medicina

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Resum

Hypotrichosis is a relatively common feature of a number of complex hereditary syndromes. However, the isolated variant, called hereditary hypotrichosis simplex (HHS), is especially uncommon. We present a Spanish family with 8 of 19 persons covering 4 generations affected by HHS. No associated ectodermal or other defects were noted. The pedigree was compatible with an autosomal dominant inheritance with variable penetrance.

Idioma original	Anglès
Pàgines (de-a)	339-342
Revista	Dermatology
Volum	196
Número	3
DOIs	https://doi.org/10.1159/000017909
Estat de la publicació	Publicada - 28 de maig 1998

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10.1159/000017909

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@article{b297e933bbf842f5849739d3a87ab19f,

title = "Hereditary hypotrichosis simplex",

abstract = "Hypotrichosis is a relatively common feature of a number of complex hereditary syndromes. However, the isolated variant, called hereditary hypotrichosis simplex (HHS), is especially uncommon. We present a Spanish family with 8 of 19 persons covering 4 generations affected by HHS. No associated ectodermal or other defects were noted. The pedigree was compatible with an autosomal dominant inheritance with variable penetrance.",

keywords = "Autosomal dominant inheritance, Hair disorder, Hereditary hypotrichosis simplex",

author = "M. Just and M. Ribera and Fuente, {M. J.} and I. Bielsa and Carlos Ferr{\'a}ndiz",

year = "1998",

month = may,

day = "28",

doi = "10.1159/000017909",

language = "English",

volume = "196",

pages = "339--342",

journal = "Dermatology",

issn = "1018-8665",

number = "3",

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TY - JOUR

T1 - Hereditary hypotrichosis simplex

AU - Just, M.

AU - Ribera, M.

AU - Fuente, M. J.

AU - Bielsa, I.

AU - Ferrándiz, Carlos

PY - 1998/5/28

Y1 - 1998/5/28

N2 - Hypotrichosis is a relatively common feature of a number of complex hereditary syndromes. However, the isolated variant, called hereditary hypotrichosis simplex (HHS), is especially uncommon. We present a Spanish family with 8 of 19 persons covering 4 generations affected by HHS. No associated ectodermal or other defects were noted. The pedigree was compatible with an autosomal dominant inheritance with variable penetrance.

AB - Hypotrichosis is a relatively common feature of a number of complex hereditary syndromes. However, the isolated variant, called hereditary hypotrichosis simplex (HHS), is especially uncommon. We present a Spanish family with 8 of 19 persons covering 4 generations affected by HHS. No associated ectodermal or other defects were noted. The pedigree was compatible with an autosomal dominant inheritance with variable penetrance.

KW - Autosomal dominant inheritance

KW - Hair disorder

KW - Hereditary hypotrichosis simplex

U2 - 10.1159/000017909

DO - 10.1159/000017909

M3 - Article

SN - 1018-8665

VL - 196

SP - 339

EP - 342

JO - Dermatology

JF - Dermatology

IS - 3

ER -

Hereditary hypotrichosis simplex

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