Ayazi syndrome

Ayazi syndrome (or Chromosome 21 Xq21 deletion syndrome)[1] is a syndrome characterized by choroideremia, congenital deafness and obesity.

Ayazi syndrome
Other namesChoroideremia-deafness-obesity syndrome
This condition is inherited in an X-linked recessive manner

Signs and symptoms

Genetics

Ayazi syndrome's inheritance pattern is described as x-linked recessive. Genes known to be deleted are CHM and POU3F4, both located on the Xq21 locus.[1]

References

Classification
External resources


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