Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia–Alania, Case Series Report

Author:

Vasilyeva Tatyana A.1,Marakhonov Andrey V.1ORCID,Tebieva Inna S.2,Kadyshev Vitaly V.1,Borovikov Artem O.1ORCID,Markova Zhanna G.1,Chukhrova Alyona L.1,Ginter Evgeny K.1,Kutsev Sergey I.1,Zinchenko Rena A.13ORCID

Affiliation:

1. Research Centre for Medical Genetics, 115522 Moscow, Russia

2. Republican Children’s Clinical Hospital, 362003 Vladikavkaz, Russia

3. N.A. Semashko National Research Institute of Public Health, 105064 Moscow, Russia

Abstract

North Caucasus has always been a residence of a lot of different authentic ethnic groups speaking different languages and still living their traditional lifestyle. The diversity appeared to be reflected in the accumulation of different mutations causing common inherited disorders. X-linked ichthyosis represents the second most common form of genodermatoses after ichthyosis vulgaris. Eight patients from three unrelated families of different ethnic origin, Kumyk, Turkish Meskhetians, and Ossetian, with X-linked ichthyosis from the North Caucasian Republic of North Ossetia–Alania were examined. NGS technology was implied for searching for disease-causing variants in one of the index patients. Known pathogenic hemizygous deletion in the short arm of chromosome X encompassing the STS gene was defined in the Kumyk family. A further analysis allowed us to establish that likely the same deletion was a cause of ichthyosis in a family belonging to the Turkish Meskhetians ethnic group. In the Ossetian family, a likely pathogenic nucleotide substitution in the STS gene was defined; it segregated with the disease in the family. We molecularly confirmed XLI in eight patients from three examined families. Though in two families, Kumyk and Turkish Meskhetian, we revealed similar hemizygous deletions in the short arm of chromosome X, but their common origin was not likely. Forensic STR markers of the alleles carrying the deletion were defined to be different. However, here, common alleles haplotype is hard to track for a high local recombination rate. We supposed the deletion could arise as a de novo event in a recombination hot spot in the described and in other populations with a recurrent character. Defined here are the different molecular genetic causes of X-linked ichthyosis in families of different ethnic origins sharing the same residence place in the Republic of North Ossetia–Alania which could point to the existing reproductive barriers even inside close neighborhoods.

Funder

state assignment of the Ministry of Science and Higher Education of the Russian Federation

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference27 articles.

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3. Steroid sulfatase deficiency causes cellular senescence and abnormal differentiation by inducing yippee-like 3 expression in human keratinocytes;Baek;Sci. Rep.,2021

4. Crane, J.S., and Paller, A.S. (2022, September 05). X-linked ichthyosis, Statpearls, Available online: https://www.ncbi.nlm.nih.gov/books/NBK448149/.

5. (2022, September 05). Orphanet Report Series—Prevalence of Rare Diseases: Bibliographic Data. Available online: http://www.orpha.net/orphacom/cahiers/docs/GB/Prevalence_of_rare_diseases_by_diseases.pdf.

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