Results 211 to 220 of about 8,285 (255)

Biallelic mutations in the LPAR6 gene causing autosomal recessive wooly hair/hypotrichosis phenotype in five Pakistani families

International Journal of Dermatology, 2019
Autosomal recessive wooly hair/hypotrichosis is an inherited disorder of hair characterized by less dense, short, and tightly curled hair on the scalp and sometimes less dense to complete absence of eyebrows and eyelashes.
G. M. Khan, Noor Hassan, Niamat Khan, M. Humayun, Kafaitullah Khan, Samira Khaliq, F. Rehman, Sheikh Ahmed, K. Shah, S. A. Khan, Noor Muhammad, A. Wali, Saadullah Khan, S. Basit, M. Ayub   +14 more
semanticscholar   +1 more source

Palmoplantar keratoderma: a new phenotype in patients with hypotrichosis resulted from lanosterol synthase gene mutations

Journal of the European Academy of Dermatology and Venereology, 2022
Y. Wang, J. Zhang, C. Pan, Q. Cao, X. Y. Wang, A. Zhao, Z. Yao, J. Han, M. Li   +8 more
semanticscholar   +1 more source

Hypotrichosis congenita hereditaria Typ M. Unna

Archiv für Dermatologie und Syphilis, 1953
Es wird uber weitere Falle der von M. Unna bereits beschriebenen erblichen Hypotrichose bei einer niedersachsischen Familie berichtet. Die Haaranomalie ist klinisch durch hochgradige angeborene Haararmut, verspatet auftretendes Wachstum borstigen Kopfhaares, fruhzeitig einsetzendem, zu fast volliger Kahlheit fuhrendem Haarausfall, histologisch (im ...
openaire   +2 more sources

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

[Genetic analysis of a child with Hypotrichosis simplex].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Yujuan Zhai, Xiaohui Li, Wei Wang, Jinfa Dou, Jianbo Wang, D. Shi   +5 more
semanticscholar   +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