PMID- 28471129
OWN - NLM
STAT- MEDLINE
DCOM- 20170606
LR  - 20170606
IS  - 1359-4117 (Print)
IS  - 1359-4117 (Linking)
VI  - 11
IP  - 3
DP  - 2016 Jul
TI  - Management of a multiple endocrine neoplasia type 1 during pregnancy: A case 
      report and review of the literature.
PG  - 217-220
AB  - Multiple Endocrine Neoplasia Type 1 (MEN1) or Wermer's syndrome is a rare 
      hereditary endocrine syndrome with high penetrance caused by mutations in MEN1 
      tumor suppressor gene. MEN1 is characterized by hyperplasia or tumoral 
      enlargement in a number of endocrine organs (parathyroid glands, pancreas, 
      pituitary gland, adrenal gland) and it could be hormonally active or inactive. 
      MEN1 is a significant cause of morbidity due to hormone secretion and mass 
      effect. Since it is a rare condition, there are no guidelines with respect to the 
      follow-up of pregnant women with MEN1. Herein, we aimed to present the diagnosis 
      and gestational follow-up of a 29-year-old pregnant with MEN1 syndrome.
CI  - (c) 2016 Old City Publishing, Inc.
FAU - Daglar, Halil Korkut
AU  - Daglar HK
AD  - Department of Perinatology, Zekai Tahir Burak Women's Health Education and 
      Research Hospital, Ankara, Turkey.
FAU - Kirbas, Ayse
AU  - Kirbas A
AD  - Department of Perinatology, Zekai Tahir Burak Women's Health Education and 
      Research Hospital, Ankara, Turkey.
FAU - Biberoglu, Ebru
AU  - Biberoglu E
AD  - Department of Perinatology, Zekai Tahir Burak Women's Health Education and 
      Research Hospital, Ankara, Turkey.
FAU - Laleli, Bergen
AU  - Laleli B
AD  - Department of Perinatology, Zekai Tahir Burak Women's Health Education and 
      Research Hospital, Ankara, Turkey.
FAU - Danisman, Nuri
AU  - Danisman N
AD  - Department of Perinatology, Zekai Tahir Burak Women's Health Education and 
      Research Hospital, Ankara, Turkey.
LA  - eng
PT  - Case Reports
PT  - Journal Article
PT  - Review
PL  - United States
TA  - J Exp Ther Oncol
JT  - Journal of experimental therapeutics & oncology
JID - 9604933
RN  - 0 (MEN1 protein, human)
RN  - 0 (Proto-Oncogene Proteins)
SB  - IM
MH  - Adult
MH  - DNA Mutational Analysis
MH  - Female
MH  - Genetic Predisposition to Disease
MH  - Humans
MH  - Live Birth
MH  - Multiple Endocrine Neoplasia Type 1/diagnosis/genetics/*therapy
MH  - Mutation
MH  - Phenotype
MH  - Pregnancy
MH  - Pregnancy Complications, Neoplastic/diagnosis/genetics/*therapy
MH  - Proto-Oncogene Proteins/genetics
MH  - Treatment Outcome
OTO - NOTNLM
OT  - calcium
OT  - insulin
OT  - parathyroid
OT  - pituitary
OT  - pregnancy
EDAT- 2017/05/05 06:00
MHDA- 2017/06/07 06:00
CRDT- 2017/05/05 06:00
PHST- 2015/09/30 00:00 [received]
PHST- 2015/12/14 00:00 [revised]
PHST- 2015/12/18 00:00 [accepted]
PHST- 2017/05/05 06:00 [entrez]
PHST- 2017/05/05 06:00 [pubmed]
PHST- 2017/06/07 06:00 [medline]
AID - 150930-AK [pii]
PST - ppublish
SO  - J Exp Ther Oncol. 2016 Jul;11(3):217-220.