PMID- 9863605
OWN - NLM
STAT- MEDLINE
DCOM- 19990322
LR  - 20190503
IS  - 0022-2593 (Print)
IS  - 1468-6244 (Electronic)
IS  - 0022-2593 (Linking)
VI  - 35
IP  - 12
DP  - 1998 Dec
TI  - Familial occurrence of congenital incomplete prepyloric mucosal diaphragm.
PG  - 1040-2
AB  - Incomplete prepyloric mucosal diaphragm (IPMD) is an uncommon congenital anomaly 
      that leads to gastric outlet obstruction in infancy and childhood. This report 
      describes the occurrence of IPMD in six children in a closely knit tribal family 
      from a geographically isolated desert town with a small population in the Sahara. 
      Their records showed similarities of clinical, radiological, operative, and 
      histopathological features. These features, as well as its occurrence in 
      brothers, sisters, and cousins, suggest that this unusual anomaly is transmitted 
      as an autosomal recessive trait.
FAU - Gahukamble, D B
AU  - Gahukamble DB
AD  - Department of Paediatric Surgery, Faculty of Medicine, Al-Arab Medical 
      University, Benghazi, Libya.
LA  - eng
PT  - Case Reports
PT  - Journal Article
PL  - England
TA  - J Med Genet
JT  - Journal of medical genetics
JID - 2985087R
SB  - IM
MH  - Child
MH  - Female
MH  - Gastric Mucosa/*abnormalities
MH  - Gastric Outlet Obstruction/*congenital/pathology
MH  - Humans
MH  - Infant
MH  - Male
MH  - Pedigree
PMC - PMC1051520
EDAT- 1998/12/24 00:00
MHDA- 1998/12/24 00:01
PMCR- 1998/12/01
CRDT- 1998/12/24 00:00
PHST- 1998/12/24 00:00 [pubmed]
PHST- 1998/12/24 00:01 [medline]
PHST- 1998/12/24 00:00 [entrez]
PHST- 1998/12/01 00:00 [pmc-release]
AID - 10.1136/jmg.35.12.1040 [doi]
PST - ppublish
SO  - J Med Genet. 1998 Dec;35(12):1040-2. doi: 10.1136/jmg.35.12.1040.