Ayazi syndrome | |
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Other names | Choroideremia-deafness-obesity syndrome |
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This condition is inherited in an X-linked recessive manner. |
Ayazi syndrome (or Chromosome 21 Xq21 deletion syndrome)[1] is a syndrome characterized by choroideremia, congenital deafness and obesity.
The presentation for this condition is as follows:[citation needed]
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]