Laddar...
Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation
von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited disorder, characterized by hemangioblastomas of the retina and central nervous system (CNS); renal cysts; clear cell carcinoma; pheochromocytoma (PCC); endolymphatic sac tumors; cystadenomas of the epididymis in males; broad ligame...
Sparad:
| I publikationen: | J Clin Res Pediatr Endocrinol |
|---|---|
| Huvudupphovsmän: | , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Galenos Publishing
2018
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5985389/ https://ncbi.nlm.nih.gov/pubmed/29022557 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.5078 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|