Menkes kinky hair disease or Menkeys disease is a rare x linked disorder causes by mutation of the ATP7A gene that regulates the metabolism of copper. Here we discuss an eight month old male infant with protein energy malnutrition who was admitted in the hospital with history of...
Open access
Research Article10.9734/ajrdes/2025/v8i1119
Werner’s Syndrome (WS) also known as Pangeria is a rare premature aging autosomal recessive disorder. It affectes the connective tissue throughout the body with high prevalence in Sardinia and Japan.The signs of premature aging appears by second to third decade of life with in...
Granulomatous cheilitis (GC) also known as Miescher cheilitis, is a rare chronic inflammatory idiopathic disorder of lips characterized by painless swelling of lips and was first described by Meischer in 1945. Wiensenfeld described it as non caseating granulomatous inflammation w...
Aim: Lymphangiomas are malformations of the lymphatic system that are located in the skin and subcutaneous tissues. We report a case of invasive lymphangioma circumscriptum successfully treated by surgery. Presentation of a Case: A 10-year female presented with asymptomatic lesio...