Richards-Rundle syndrome (Q60243): Difference between revisions
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| description / pt-br | description / pt-br | ||
Síndrome de Richards-Rundle é um transtorno muito raro caracterizado por ataxia autossômica recessiva, perda auditiva, deterioração mental, perda muscular periférica, hipogonadismo hipergonadotrófico e cetoacidúria. | |||
| description / en | description / en | ||
Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria. | |||
Revision as of 07:45, 14 August 2026
Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_114583632 |
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| English | Richards-Rundle syndrome |
Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria. |
