Ontology highlight
ABSTRACT:
SUBMITTER: Saleh Anaraki K
PROVIDER: S-EPMC9051674 | biostudies-literature | 2022 Mar
REPOSITORIES: biostudies-literature
Saleh Anaraki Kimia K Khosravi Sepehr S Behrangi Elham E Sadeghzadeh-Bazargan Afsaneh A Goodarzi Azadeh A
Journal of family medicine and primary care 20220310 3
H syndrome is a systemic inherited autosomal recessive histiocytosis, with characteristic cutaneous findings accompanying systemic manifestations and a most common genetic mutation (OMIM 612391) as SLC29A3. The term "H Syndrome" is representative of presentation with hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and, occasionally, hyperglycemia. H syndrome is new and growing entity in medicine. This syndrome is not specific to a r ...[more]