Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome Sequencing

Author:

Mezzi NessrineORCID,Zaouak AnissaORCID,Mkaouar RahmaORCID,Kacem Imen,Gouider Riadh,Fenniche Samy,Mrad Ridha,Abdelhak SoniaORCID,Romdhane LiliaORCID

Publisher

Elsevier BV

Reference16 articles.

1. Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child;Benmously‐Mlika;Int. J. Dermatol.,2014

2. Specific TGM1 mutation profiles in bathing suit and self-improving collodion ichthyoses: phenotypic and genotypic data from 9 patients with dynamic phenotypes of autosomal recessive congenital ichthyosis;Bourrat;Arch. Dermatol.,2012

3. Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parents;Durdu;BMC Med. Genet.,2018

4. Genetic analysis of muscular dystrophies: our experience in Mexico;Escobar-Cedillo;Folia Neuropathol.,2021

5. Hentati, F., 2008. Muscular dystrophies in Arab countries. The First Educational Workshop in Developing Countries on Genetic Counseling, Beirut, Lebanon.

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