The ABCD syndrome denotes albinism, black lock, cell migration of the gut which involves neurocytes, and the deafness which is sensorinueral. The mutation in the gene is responsible for it.
It is characterized by the albinism, black lock at the temporal occipital region. It was studied in the Kurdish girl. She had white eye brows and eyelashes. She had blue
In the Europe waarndenburg syndrome occurs in one in 45000 people. The diagnosis is made before the birth by ultrasound. It occurs due to the phenotype which displays disturbances in the face,
