Φορτώνει......
Endocrinological and phenotype evaluation in a patient with acrodysostosis
Acrodysostosis is characterized by distinctive facial features and severe brachydactyly. Mutations in PRKAR1A or PDE4D are known to be responsible for this disease. Cases of hormonal resistance have been reported, particularly in patients with PRKAR1A mutations. The physical characteristics and endo...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Clin Pediatr Endocrinol |
|---|---|
| Κύριοι συγγραφείς: | , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
The Japanese Society for Pediatric
Endocrinology
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5537214/ https://ncbi.nlm.nih.gov/pubmed/28804209 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.26.177 |
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