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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Med Case Rep |
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| Κύριοι συγγραφείς: | , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2019
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| Θέματα: | |
| Διαθέσιμο Online: | 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 |
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