Diagnosis of primary hyperparathyroidism (PHPT) is a challenging issue in some cases because of the uncommon and various presentations. Primary hyperparathyroidism is a relatively common condition, originating from parathyroid adenomas, with a prevalence of 25 per 100,000 people....
Open access
Research Article10.9734/IJMPCR/2015/19647
Introduction: Macrophage Activation Syndrome (MAS) is a rare and life-threatening complication of various chronic rheumatic diseases. It is associated with systemic-onset juvenile idiopathic arthritis (SoJIA). Case Report: A 19-year old woman was referred to our hospital with a h...
Open access
Research Article10.9734/IJMPCR/2015/18921
Background: Alkaptonuria (AKU), also known as black urine disease, ochronosis as well, is a rare Mendelian autosomal recessive disorder, located on chromosome 3q21-q23, caused by deficiency of the homogentisate 1,2 dioxygenase (HGO), an enzyme which normally catalyses the conve...
Open access
Research Article10.9734/IJMPCR/2016/22710