Results 191 to 200 of about 3,476 (222)

Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging

, 2013
Kyle B. Jones, Alice F. Goodwin, Maya Landan, Kerstin Seidel, Dong‐Kha Tran, Jacob S. Hogue, Miquella G. Chavez, Mary Fete, YU Wen-li, Tarek Hussein, Ramsey Johnson, Kenneth Huttner, Andrew H. Jheon, Ophir D. Klein   +13 more
openalex   +1 more source

Correction: Methylation State of the EDA Gene Promoter in Chinese X-Linked Hypohidrotic Ectodermal Dysplasia Carriers

, 2013
Wei Yin, Xiaoqian Ye, Huali Fan, Zhuan Bian   +3 more
openalex   +2 more sources

Early recognition of hypohidrotic ectodermal dysplasia

Head & Face Medicine, 2012
Schneider Holm
doaj   +1 more source

A rare case of X-linked hypohidrotic ectodermal dysplasia with chorioretinal lesions by missense mutation in ectodysplasin A gene from Northeast India

Nilutparna Deori, Madhusmita Mahapatra, Dipankar Das, Manjisa Choudhury   +3 more
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Hypohidrotic ectodermal dysplasia with autosomal recessive inheritance pattern: Report of a rare and unusual case with a brief review of literature.

J Oral Maxillofac Pathol, 2019
Hasan S, Govind M, Sawai MA, Ansari MD.
europepmc   +1 more source

Hypohidrotic Ectodermal Dysplasia With Bronchial Asthma - A Rare Association

, 2005
Usha Gupta, Krishna Deb Barman, Khozema Saify, Dinesh Gupta, Sachin Luthra   +4 more
openalex   +1 more source

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A Case of Hypohidrotic Ectodermal Dysplasia

The Journal of Dermatology, 1999
AbstractHypohidrotic ectodermal dysplasia (HED) is a rare, hereditary, congenital disease that affects several ectodermal structures. It is characterised by the following: anhidrosis or hypohidrosis, dental abnormalities, hypotrichosis, and a characteristic facies.
J W, Park, J Y, Hwang, S Y, Lee, J S, Lee, M K, Go, K U, Whang   +5 more
openaire   +2 more sources

Hypohidrotic ectodermal dysplasia with hypothyroidism

The Journal of Pediatrics, 1981
Two brothers with hypohidrotic ectodermal dysplasia were found to have urticaria pigmentosa-like skin pigmentation with increased mast cells and melanin depositions in the dermis. Structural ciliary abnormalities of the respiratory tract were seen, and these may contribute to their severe recurrent chest infections.
H F, Pabst, O, Groth, E E, McCoy
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Hypohidrotic Ectodermal Dysplasia and Intrathoracic Neuroblastoma

Pediatric Dermatology, 2007
Abstract:  We report a 6‐year‐old girl with a subtle form of hypohidrotic ectodermal dysplasia and a phenotype consisting of curly hair, a round face, a stocky build, and obesity, which was associated with intrathoracic neuroblastoma. Although this new association could be a chance occurrence, its description may alert physicians to look for similar ...
Buoni S, Zannolli R, Macucci F, Molinelli M, Viviano M, Cuccia A, Hayek J, VOLTERRANI, LUCA, de Santi MM, MIRACCO, CLELIA, Fois A.   +10 more
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