A patient with bilateral pheochromocytoma as part of a Von Hippel-Lindau (VHL) syndrome type 2C. [electronic resource]
Producer: 20080205Description: 112 p. digitalISSN:- 1477-7819
- Adrenal Gland Neoplasms -- diagnosis
- Adrenalectomy -- methods
- Adult
- Cesarean Section
- Female
- Follow-Up Studies
- Germ-Line Mutation
- Humans
- Infant, Newborn
- Infant, Premature
- Infant, Small for Gestational Age
- Magnetic Resonance Imaging
- Mutation, Missense
- Pheochromocytoma -- diagnosis
- Pregnancy
- Pregnancy Complications, Neoplastic -- diagnosis
- Pregnancy Outcome
- Pregnancy Trimester, Second
- Prenatal Diagnosis -- methods
- Risk Assessment
- Treatment Outcome
- von Hippel-Lindau Disease -- genetics
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Publication Type: Case Reports; Journal Article
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