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Coexistence of molybdenum cofactor deficiency type A and hypertrophic pyloric stenosis, a new case
Molybdenum cofactor deficiency is a rare neurometabolic disease that is usually characterized by seizures, abnormal muscle tonus, developmental delay and poor nutrition, and is seen soon after birth. Pyloric stenosis causes serious vomiting in the first months of life. The presence of neurologic dam...
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| Publicado no: | Turk Arch Pediatr |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Turkish Pediatric Association
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8114604/ https://ncbi.nlm.nih.gov/pubmed/34013236 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14744/TurkPediatriArs.2020.57984 |
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