Results 171 to 180 of about 5,635 (205)

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

Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes

American Journal of Medical Genetics, Part A, 2021
Regina Betz, Cristina Has, Fitnat Buket Basmanav   +2 more
exaly  

Hypotrichosis and Hair Loss on the Occipital Scalp

Cutis, 2023
Erica Possa, de Abreu, Vanessa Barreto, Rocha, Raquel Ferreira, Queiroz de Melo, Luciana Baptista, Pereira   +3 more
openaire   +2 more sources

Hypotrichosis

2020
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

The first reported case of CDH3-related hypotrichosis with juvenile macular dystrophy from Jordan: a case report

Ophthalmic Genetics, 2022
Hamzeh Mohammad Alrawashdeh, Nesrin Mwafi   +1 more
exaly  

Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis

Pediatric Dermatology, 2011
Khalid Al, Aboud, Daifullah Al, Aboud
openaire   +2 more sources

Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32

Clinical Genetics, 2007
Wasim Ahmad
exaly  

Hypotrichosis

2008
openaire   +1 more source