An Indian family of multiple endocrine neoplasia type 1 (MEN1): molecular diagnosis, treatment and follow up

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal, dominant syndrome, characterized mainly by the combination of tumors involving the parathyroid, pancreatic and pituitary glands. Genetic sequencing leading to early treatment of family members has not yet been reported in Indian patients. W...

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Veröffentlicht in:	Indian journal of gastroenterology 2008-11, Vol.27 (6), p.242-244
Hauptverfasser:	Shah, Sudeep R, Raghavan, Rani, Desai, Devendra C, Chauhan, Phulrenu H, Lala, Murad, Dherai, Alpa J, Ashavaid, Tester F
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Case-Control Studies Female Follow-Up Studies Humans India Male Multiple Endocrine Neoplasia Type 1 - diagnosis Multiple Endocrine Neoplasia Type 1 - genetics Multiple Endocrine Neoplasia Type 1 - therapy Mutation Pedigree Polymerase Chain Reaction
Online-Zugang:	Volltext
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