Atypical hypotonia-cystinuria syndrome (Q66532): Difference between revisions
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Uma afecção caracterizada por hipotonia neonatal e infantil, má alimentação em recém-nascidos, retardo de crescimento devido à deficiência de hormônio do crescimento, dismorfismo facial leve e cistinúria tipo I. | |||
| description / en | description / en | ||
A condition characterised by neonatal and infantile hypotonia, poor feeding in neonates, growth retardation due to growth hormone deficiency, mild facial dysmorphism and cystinuria type I. | |||
Revision as of 14:21, 14 August 2026
A condition characterised by neonatal and infantile hypotonia, poor feeding in neonates, growth retardation due to growth hormone deficiency, mild facial dysmorphism and cystinuria type I.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1982772708 |
||
| English | Atypical hypotonia-cystinuria syndrome |
A condition characterised by neonatal and infantile hypotonia, poor feeding in neonates, growth retardation due to growth hormone deficiency, mild facial dysmorphism and cystinuria type I. |
