Category: Genetics and Birth Defects
Encephalocele is a debilitating condition that is frequently associated with a host of cranial and facial abnormalities. Read and know more about the types, symptoms, causes, diagnosis, treatment and …
Krabbe Disease is a rare genetic disorder that often turns fatal for its sufferers. Read and know what this condition is like, what are its causes, how it can …
Adrenoleukodystrophy (ALD) is one of the most common genetic disorders affecting 1 in every 17000 newborns in the US. Learn all about this abnormal condition and get detailed information …
Coarctation of the aorta is one of the most common cardiac defects and is responsible for 5-8% of all congenital heart problems. Learn all about this abnormal cardiac disorder, …
Holt Oram Syndrome is a genetic disease that impacts physical development and also gives rise to cardiac problems. Find out all about this condition, including its causes, symptoms, diagnosis …
Waardenburg Syndrome (WS) is a rare hereditary disease that leads to loss of hearing in varying degrees as well as various other physical problems. Read on to get detailed …
Muckle-Wells Syndrome (MWS) is a rare type of genetic disease that is characterized by occasional occurrences of skin rash, fever and joint pain as well as various other problems. …
Imagine living without a single tooth in the prime of your life. A disorder known as Anodontia is manifested by such toothless condition in its patients. Read and find …
Aicardi Syndrome is a rare life-threatening disorder that mainly affects girl children around the world. Read and know all about the causes, symptoms, diagnosis and treatment of this disorder. …
What is Fetal Hydantoin Syndrome? Fetal Hydantoin Syndrome or Fetal Dilantin Syndrome is a rare disease that is caused when a fetus is exposed to Phenytoin, an anticonvulsant drug …