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X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus
- Source :
- Scopus-Elsevier, Human genetics, 87(6), 661-664. Springer Verlag
- Publication Year :
- 1991
- Publisher :
- Springer Science and Business Media LLC, 1991.
-
Abstract
- A case of X-linked recessive chondrodysplasia punctata (CP) is described. The finding of a reciprocal X-Y translocation involving the region distal to Xp22.3 and the presence of fluorescent Yp11.23 regions confirms the localization of X-linked recessive CP at p22.3. No gross peroxisomal abnormalities were present in the propositus.
- Subjects :
- Adult
Male
musculoskeletal diseases
Chondrodysplasia Punctata
congenital, hereditary, and neonatal diseases and abnormalities
X Chromosome
Genetic Linkage
Genes, Recessive
Chromosomal translocation
Biology
Microbodies
Translocation, Genetic
Y Chromosome
X-linked recessive chondrodysplasia punctata
Genetics
medicine
Humans
Chondrodysplasia punctata
Fetal Death
Genetics (clinical)
Fetus
Ichthyosis
Chromosome
DNA
musculoskeletal system
medicine.disease
Immunohistochemistry
Osteochondrodysplasia
Karyotyping
Recien nacido
Female
sense organs
human activities
Subjects
Details
- ISSN :
- 14321203 and 03406717
- Volume :
- 87
- Database :
- OpenAIRE
- Journal :
- Human Genetics
- Accession number :
- edsair.doi.dedup.....3f8fec9b60b25a8bbb9a44642fcd048e
- Full Text :
- https://doi.org/10.1007/bf00201721