Three distinct types of X-linked arthrogryposis seen in 6 families.
Six families with arthrogryposis (congenital contractures) inherited in an X-linked recessive manner are reported. Family histories from a study of over 350 patients with congenital contractures of the joints (arthrogryposis) were reviewed and of these, three probands had family histories consistent with X-linked recessive inheritance. Three other families were recognized through correspondence. Three forms of X-linked recessively inherited arthrogryposis are described: (1) Severe lethal X-linked arthrogryposis with severe contractures scoliosis deformities, hypotonia, and death due to respiratory insufficiency within 3 months of birth (1 family); (2) Moderately severe X-linked arthrogryposis with severe contractures, ptosis, microphallus, cryptorchidism, inguinal hernias, and normal intelligence (2 families); and (3) Resolving X-linked arthrogryposis with mild to moderate contractures at birth which improve dramatically with time (2 families and 1 sporadic case).
Duke Scholars
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- X Chromosome
- Sex Chromosomes
- Phenotype
- Pedigree
- Male
- Infant, Newborn
- Infant
- Humans
- Genetics & Heredity
- Genetic Linkage
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- X Chromosome
- Sex Chromosomes
- Phenotype
- Pedigree
- Male
- Infant, Newborn
- Infant
- Humans
- Genetics & Heredity
- Genetic Linkage