There is 29 Article with tag "Congenital Disorders"
Carpenter syndrome is a rare genetic disorder that runs in families. To date, only about 70 cases have been reported globally.
Osteogenesis imperfecta (OI) is a congenital (genetic) bone disorder that is present at birth.
Sacrococcygeal teratoma is a tumor condition that grows from the tailbone in newborns.
Ellis-van Creveld syndrome (EVC) is a rare genetic disease that leads to impaired bone growth.
Pelvic dysplasia is a condition in which the “ball and socket” joint of the hip does not form properly in infants and young children.
Duchenne Muscular Dystrophy, or DMD, is a congenital disease caused by genetic mutation.
Torticollis is a condition characterized by the twisting of a baby's neck muscles, resulting in the appearance of the head being inclined to one side only.
Spina bifida is a congenital disorder in which an abnormal bone and spinal cord formation occurs.
Movement Mirror Disorder (MMD) or Congenital Mirror Movement Disorder (CMMD) is a rare neurological condition.
Get to know the causes, symptoms, prevention methods, complications and management of microcephaly.
Congenital abnormalities are structural or functional disorders that occur during fetal life.