Hypotonia-cystinuria syndrome (Q63719): Difference between revisions
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A síndrome hipotonia-cistinúria é uma síndrome rara, incluindo hipotonia neonatal e infantil, cistinúria tipo 1 e nefrolitíase, retardo de crescimento devido à deficiência de hormônio do crescimento e dismorfismo facial menor. | |||
| description / en | description / en | ||
Hypotonia-Cystinuria syndrome is a rare syndrome including neonatal and infantile hypotonia and failure to thrive, cystinuria type 1 and nephrolithiasis, growth retardation due to growth hormone deficiency, and minor facial dysmorphism. | |||
Revision as of 11:13, 14 August 2026
Hypotonia-Cystinuria syndrome is a rare syndrome including neonatal and infantile hypotonia and failure to thrive, cystinuria type 1 and nephrolithiasis, growth retardation due to growth hormone deficiency, and minor facial dysmorphism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1742079513 |
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| English | Hypotonia-cystinuria syndrome |
Hypotonia-Cystinuria syndrome is a rare syndrome including neonatal and infantile hypotonia and failure to thrive, cystinuria type 1 and nephrolithiasis, growth retardation due to growth hormone deficiency, and minor facial dysmorphism. |
