Results 221 to 230 of about 7,293 (261)

Neonatal ichthyosis and hypotrichosis

Pediatric Dermatology, 2019
Pedro Vilas Boas, Alejandro Sanchez‐Herrero, Ricardo Suárez‐Fernández, Minia Campos‐Dominguez   +3 more
openaire   +2 more sources

Congenital hypotrichosis

International Journal of Dermatology, 1999
openaire   +2 more sources

Congenital hereditary hypotrichosis(Marie Unna hypotrichosis). Report of two cases

1980
We report two patients, mother and daughter, presenting a Marie Unna's syndrome and belonging to a family in which the disease appeared in seven members in a period of four generations. We point out the more frequent features of this syndrome: male pattern alopecia, rare hairs resembling a 'horse hair', and follicular atrophy.
S.Menni, C.Crosti
openaire   +1 more source

Hypotrichosis, milia, brachydactyly, and frenula

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2015
Antonia, Jeskowiak, Thomas A, Luger, Markus, Böhm   +2 more
openaire   +2 more sources

Hypotrichosis

2020
openaire   +1 more source

Diffuse hypotrichosis from early childhood

Journal of the American Academy of Dermatology, 2016
Ángela, Hermosa-Gelbard, David, Saceda-Corralo, Juan Ferrando, Barbera, Sergio, Vañó-Galván   +3 more
openaire   +2 more sources

The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X‐linked hypohidrotic ectodermal dysplasia: A systematic review

American Journal of Medical Genetics, Part A, 2020
Erin P Carmany
exaly  

Hyperpigmented Flexural Plaques, Hypohidrosis, and Hypotrichosis

Cutis, 2023
India A, Loyd, Amanda S, Weissman, Jarad, Levin   +2 more
openaire   +2 more sources

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

Nature Genetics, 2003
Regina Betz, Michel Simon, Axel M Hillmer   +2 more
exaly  

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin

Nature Genetics, 2001
Eli Sprecher, Ido Perlman
exaly