1.
Ceylon Med J
;
2001 Mar; 46(1): 30
Article
in English
| IMSEAR
| ID: sea-47917
ABSTRACT
Meckel Gruber syndrome (MGS), an autosomal recessive disorder characterised by posterior encephalocoele, multicystic kidneys and post-axial polydactyly should be recognised by obstetricians and paediatricians to counsel parents regarding the 25% recurrence risk. We report a consanguineous family with MGS affecting three infants.
Subject(s)
Abnormalities, Multiple/diagnosis , Autopsy , Consanguinity , Encephalocele/complications , Fatal Outcome , Female , Fetal Death/etiology , Fetal Growth Retardation/etiology , Genetic Counseling , Humans , Infant, Newborn , Oligohydramnios/etiology , Polycystic Kidney Diseases/complications , Polydactyly/complications , Pregnancy , Risk Factors , Syndrome , Ultrasonography, Prenatal
2.
Ceylon Med J
;
1997 Jun; 42(2): 112
Article
in English
| IMSEAR
| ID: sea-48281