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Article

Renal Involvement in H Syndrome, A Rare Cause of Diabetes Mellitus: Case Report.

Endocrine, metabolic & immune disorders drug targets - 1 Jan 2023

Polat Recep, Ustyol Ala, Altunbaş Rabia, Ceylaner Serdar

Abstract excerpt

BACKGROUND: H syndrome is a rare genodermatosis deriving from a mutation in the SLC29A3 gene and affecting numerous systems, particularly the skin. The syndrome exhibits different clinical characteristics involving several systems, most beginning with the letter "H." The most common clinical findings are cutaneous hyperpigmentation, flexion contracture in the fingers, hearing loss, short stature,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 36372920
DOI: 10.2174/1871530323666221111151455

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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