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SynopsisCodesBest TestsReferences
Rozycki syndrome
Other Resources UpToDate PubMed

Rozycki syndrome

Other Resources UpToDate PubMed

Synopsis

An autosomal recessive genetic disorder with achalasia, congenital deafness, short stature, vitiligo, and muscle wasting.

Codes

ICD10CM:
Q87.19 – Other congenital malformation syndromes predominantly associated with short stature

SNOMEDCT:
95828007 – Congenital deafness

Best Tests

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References

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Last Updated:01/23/2022
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Rozycki syndrome
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A medical illustration showing key findings of Rozycki syndrome : Deafness, Hypopigmented patch, Muscle atrophy, Dysphagia, Cachexia
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