Hirschsprung disease - deafness - polydactyly (Q53644): Difference between revisions
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Síndrome de doença de Hirschsprung-polidactilia-surdez é uma associação de malformações extremamente rara. Os recém-nascidos também apresentaram agenesia renal unilateral e hipertelorismo. | |||
| description / en | description / en | ||
Hirschsprung disease-polydactyly-deafness syndrome is an extremely rare malformative association. The newborns also had unilateral renal agenesis and hypertelorism. | |||
Revision as of 01:12, 14 August 2026
Hirschsprung disease-polydactyly-deafness syndrome is an extremely rare malformative association. The newborns also had unilateral renal agenesis and hypertelorism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_173144974 |
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| English | Hirschsprung disease - deafness - polydactyly |
Hirschsprung disease-polydactyly-deafness syndrome is an extremely rare malformative association. The newborns also had unilateral renal agenesis and hypertelorism. |
