Abstract |
We report on a family in which two of the three children (girl and boy) have a MCA/MR syndrome consisting of peculiar facies, retarded psychomotor development, mental retardation, congenital heart defect, kyphoscoliosis, diastasis recti, and cryptorchidism in the boy. This syndrome is quite similar to that of the only family previously described and which was denominated McDonough Syndrome. The syndrome is delineated and autosomal recessive inheritance is suggested as the most likely etiology. A balanced translocation (X; 20) in the affected boy and in the unaffected mother was a coincidental finding.
|
Authors | J M García-Sagredo, C Lozano, P Ferrando, C San Román |
Journal | Clinical genetics
(Clin Genet)
Vol. 26
Issue 2
Pg. 117-24
(Aug 1984)
ISSN: 0009-9163 [Print] Denmark |
PMID | 6147215
(Publication Type: Case Reports, Comparative Study, Journal Article)
|
Topics |
- Abnormalities, Multiple
(genetics)
- Adolescent
- Adult
- Child
- Chromosomes, Human, 19-20
- Cryptorchidism
(genetics)
- Face
(abnormalities)
- Female
- Heart Defects, Congenital
(genetics)
- Humans
- Intellectual Disability
(genetics)
- Male
- Pedigree
- Syndrome
- Translocation, Genetic
- X Chromosome
|