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Definition

An autosomal recessive syndrome characterized by albinism, black lock at temporal occipital region, bilateral deafness, aganglionosis of the large intestine and total absence of neurocytes and nerve fibers in the small intestine.

Acronym

ABCDS

Synonyms

Albinism, black lock, cell migration disorder of the neurocytes of the gut and deafness

Keywords

Albinism
Deafness
Hirschsprung disease

 
Disclaimer

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