A carregar...
Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report
BACKGROUND: Familial glucocorticoid deficiency is a rare autosomal recessive disorder characterized by isolated glucocorticoid deficiency. Most patients are diagnosed following episodes of hypoglycemia or convulsion. We report the case of an infant with familial glucocorticoid deficiency who present...
Na minha lista:
| Publicado no: | J Med Case Rep |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6724328/ https://ncbi.nlm.nih.gov/pubmed/31481085 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-019-2206-5 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|