Mesomelic dysplasia, type langer?A homozygous state for dyschondrosteosis
- 1 September 1980
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 134 (3) , 269-272
- https://doi.org/10.1007/bf00441485
Abstract
Both parents of a female infant with mesomelic dysplasia, type Langer, showed signs of dyschondrosteosis. This further observation suggests that this type of mesomelic dysplasia may be due to homozygosity for the autosomal dominant gene of dyschondrosteosis.This publication has 19 references indexed in Scilit:
- Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosisHuman Genetics, 1979
- Mesomelic Dwarfism as the Homozygous Expression of DyschondrosteosisArchives of Pediatrics & Adolescent Medicine, 1975
- Dyschondrosteosis(mesomelic dwarfism)—A family studyThe British Journal of Radiology, 1974
- Dyschondrosteosis. A Mexican family with two affected malesClinical Genetics, 1972
- DyschondrosteosisActa Radiologica. Diagnosis, 1971
- DyschondrosteoseAmerican Journal of Diseases of Children, 1970
- Madelung's Deformity: Observations in 17 PatientsRadiology, 1969
- Mesomelic Dwarfism of the Hypoplastic Ulna, Fibula, Mandible TypeRadiology, 1967
- DyschondrosteosisThe Journal of Pediatrics, 1966
- DYSCHONDROSTEOSIS, A HEREDITABLE BONE DYSPLASIA WITH CHARACTERISTIC ROENTGENOGRAPHIC FEATURESAmerican Journal of Roentgenology, 1965