Meckel syndrome in different populations
- 1 August 1984
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 18 (4) , 661-669
- https://doi.org/10.1002/ajmg.1320180413
Abstract
We report on 18 infants from 13 families where the infant was affected with the Meckel syndrome. The parents belong to various national groups—Russians, Byelorussians, Poles, Ukrainians, Letts, and Tatars. One child was from an incestuous union (half‐sister and half‐brother), in 4 families the parents were natives of the same or neighboring villages; other parents apparently were not related. Excluding 3 couples from Central Russia, the Ukraine, and Tatary, the other 10 families were the inhabitants of the Moscow region, Byelorussia, and Latvia. In 3 of these families at least one grandparent was of Tatar descent. At the same time the frequency of Tatars in these regions is less than 1%. Using the Newton binomial distribution it was shown that the hypothesis about equal frequency of the Meckel syndrome gene among Tatars and other national groups under study may be excluded completely, and therefore the alternative hypothesis about an unusually high frequency of this gene among Tatars must be accepted. Such analysis may be useful for comparative evaluation of gene frequencies in populations which cannot be studied directly.Keywords
This publication has 13 references indexed in Scilit:
- Survival and spectrum of anomalies in the meckel syndromeAmerican Journal of Medical Genetics, 1983
- The Meckel syndrome. Pathological and cytogenetic observations in eight casesHuman Genetics, 1982
- Phenotypic variation in Meckel syndromeClinical Genetics, 1981
- Prenatal morphology in meckel's syndrome (with special reference to polycystic kidneys and double encephalocele)Prenatal Diagnosis, 1981
- The hydrolethalus syndrome: delineation of a “new”, lethal malformation syndrome based on 28 patientsClinical Genetics, 1981
- Sjögren‐Larsson syndrome in Sweden. A clinical, genetic and epidemiological studyClinical Genetics, 1981
- Spectrum of anomalies in the Meckel syndrome, or: “Maybe there is a malformation syndrome with at least one constant anomaly”American Journal of Medical Genetics, 1981
- The meckel syndrome in the HutteritesAmerican Journal of Medical Genetics, 1980
- Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance.Journal of Medical Genetics, 1971
- GENETICS OF THE MECKEL SYNDROME (DYSENCEPHALIA SPLANCHNOCYSTICA)Pediatrics, 1971