Report of an Iranian child with chronicabdominal pain and constipation diagnosedas glycogen storage disease type IX: a casereport Abstract
Abstract :Background: Beta-thalassemia is common in the Mediterranean area as well as the Middle East and India. Official report
Abstract :Background: It is estimated about 7% of the world population is carriers of hemoglobin diseases. Alpha‐thalassemia is one
Abstract :Introduction: Laing early-onset distal myopathy is a disorder with autosomal dominant inheritance pattern caused by a mutation in
Abstract :Introduction: Congenital hearing loss is the most common sensory deficit in the world and mutations in GJB2 gene
Background: -e human CYP2B subfamily consists of one functional gene (CYP2B6) and one pseudogene (CYP2B7P). Cytochrome P450 2B6 (CYP2B6)
SUMMARY :Background: Phenylketonuria (PKU) is the most common aminoacidopathy with an autosomal recessive inheri-tance pattern. A global PKU prevalence
SUMMARY :Background: Human papilloma viruses are a group of the Papillomaviridae family (ds DNA viruses), which infect basal epithelial
Introduction: β-Thalassaemia is the most common genetic disorder and is considered as a major public health concern in Iran.
Abstract :Background Glycogen storage disease type IX is a rare disorder that can cause a wide variety of symptoms