Ahmed Ahmed Touni*, Sherif Shoukry Awad
H syndrome, a rare genetic disorder, is inherited in an autosomal recessive manner. SLC29A3 gene mutation represents the underlying etiology of this syndrome which manifests with various cutaneous and extracutaneous features including hyperpigmentation, sclerosis, hypertrichosis. hyperglycemia, hearing loss, hypogonadism, cardiac anomalies and skeletal deformities.
Published Date: 2021-03-04; Received Date: 2021-02-11