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Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child: a case report
INTRODUCTION: Familial glucocorticoid deficiency, or hereditary unresponsiveness to adrenocorticotropic hormone, is a rare autosomal recessive disease characterized by glucocorticoid deficiency in the absence of mineralocorticoid deficiency. It may present in infancy or early childhood with hyperpig...
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3369203/ https://ncbi.nlm.nih.gov/pubmed/22507176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-6-110 |
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