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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

Ectodermal dysplasia (ED) is a congenital disorder primarily affecting the ectodermal tissue, with infrequent dysfunction of mesodermally derived tissues. Clinically, there are two major forms seen, hypohidrotic/Christ–Siemens–Touraine syndrome and hidrotic/Clouston syndrome, depending on the number...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Oral Maxillofac Pathol
Päätekijät: Hasan, Shamimul, Govind, Murali, Sawai, Madhuri Alankar, Ansari, Mohammad Dilshad
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Wolters Kluwer - Medknow 2019
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6948050/
https://ncbi.nlm.nih.gov/pubmed/31942145
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jomfp.JOMFP_98_19
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