Congenital Hepatic Fibrosis (CHF) is a rare disease that affects both the liver and kidneys.  Congenital hepatic fibrosis (CHF) is an autosomal recessive inherited malformation defined pathologically by a variable degree of periportal fibrosis and irregularly shaped proliferating bile ducts. Affected individuals also have impaired renal function, usually caused, in children and teenagers, by an...

INTRODUCTION Congenital insensitivity to pain (CIP) is a rare disorder, and often presents to an orthopaedic surgeon as recurrent fractures, dislocations, pseudoarthrosis, osteomyelitis etc. Here, we report a case of congenital insensitivity to pain presenting with distal femoral physeal separation in a child. CASE REPORT A 12-year-old girl child came with complaints of limp while walking and...

Zellweger syndrome (ZS) is a rare autosomal recessive inherited disorder within the spectrum of peroxisome biogenesis disorders. It is a progressive and fatal disorder with multiple congenital anomalies. There may be some challenges for anesthesiologists in patients with ZS. We report the anesthetic management of an infant with ZS undergoing closure of patent ductus arteriosus and pulmonary art...

hemimelia as a congenital anomaly is a failure of development of extremities formation in embryonic period. this anomaly is defined as complete absence of the part of extremities and different forms were explained for hemimelia. adactyly is an alternative name for transverse hemimelia and is a rare disorder in the most of animal species. a two months old male lamb with normal vital signs was re...

Congenital disorders are a group of rare diseases and one the health problems that often overlooked. disorder needs to get more attention because it can affect quality life patient affected family. Because its impact on patient's in future, early detection is needed be able provide intervention minimize long-term effects. Doctors who work primary facilities have an important role congenital abn...