Ghaith Abdessalem
Tunis, Tunisia
Last Updated: 09/26/2026
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Found 8 publications
Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis.
Journal: International journal of women's dermatology
Published: February 05, 2024
When to Recommend a Peripheral Blood Smear to Patients with Congenital Ichthyosiform Erythroderma.
Journal: Skinmed
Published: August 17, 2022
Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved.
Journal: Genes
Published: September 27, 2021
Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family.
Journal: Journal of human genetics
Published: March 22, 2019
Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus.
Journal: Bioscience reports
Published: December 15, 2018
Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM1 gene.
Journal: International journal of dermatology
Published: December 13, 2018
A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene.
Journal: International journal of dermatology
Published: June 28, 2018
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Last Updated: 09/26/2026