The long-term objectives of this study are to continue to establish the developmental prognosis into adulthood of individuals with sex chromosome abnormalities (SCA) identified at birth in an unselected fashion between 1964 and 1974. In the course of this longitudinal study, we have documented the physical, endocrine, developmental, and psychological phenotypes of SCA children. The presence of language, learning, and neuromotor impairment in SCA children and of psychosocial dysfunction in SCA adolescents suggests that SCA adults are at risk for difficulty in social and vocational adaptation and may experience increased incidence of psychopathology. No studies of an unselected SCA adult cohort are in existence, and the absence of any newborn sex chromosome screening programs in the past two decades indicates that the Denver Study will be the first and possibly last foreseeable opportunity to study adult adaptation in this population. This proposal includes investigations of physical, endocrine, neurocognitive, vocational, and psychosocial characteristics of 42 SCA propositi and a control group that includes 32 siblings.
The specific aims allow us to address questions raised in our earlier studies of this group and to complete the phenotypic profile from birth into adulthood of the 45,X, 47,XXX, 47,XXY, and sex chromosome mosaic karyotypes.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
2R01HD010032-16A1
Application #
3311216
Study Section
Human Development and Aging Subcommittee 3 (HUD)
Project Start
1976-05-01
Project End
1995-07-31
Budget Start
1992-08-01
Budget End
1993-07-31
Support Year
16
Fiscal Year
1992
Total Cost
Indirect Cost
Name
National Jewish Health
Department
Type
DUNS #
City
Denver
State
CO
Country
United States
Zip Code
80206
Patwardhan, Anil J; Brown, Wendy E; Bender, Bruce G et al. (2002) Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes. Am J Med Genet 114:93-8
Linden, Mary G; Bender, Bruce G; Robinson, Arthur (2002) Genetic counseling for sex chromosome abnormalities. Am J Med Genet 110:3-10
Linden, Mary G; Bender, Bruce G (2002) Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities. Am J Med Genet 110:11-8
Bender, B G; Linden, M G; Harmon, R J (2001) Life adaptation in 35 adults with sex chromosome abnormalities. Genet Med 3:187-91
Bender, B G; Linden, M G; Harmon, R J (2001) Neuropsychological and functional cognitive skills of 35 unselected adults with sex chromosome abnormalities. Am J Med Genet 102:309-13
Patwardhan, A J; Eliez, S; Bender, B et al. (2000) Brain morphology in Klinefelter syndrome: extra X chromosome and testosterone supplementation. Neurology 54:2218-23
Harmon, R J; Bender, B G; Linden, M G et al. (1998) Transition from adolescence to early adulthood: adaptation and psychiatric status of women with 47,XXX. J Am Acad Child Adolesc Psychiatry 37:286-91
Linden, M G; Bender, B G; Robinson, A (1996) Intrauterine diagnosis of sex chromosome aneuploidy. Obstet Gynecol 87:468-75
Linden, M G; Bender, B G; Robinson, A (1995) Sex chromosome tetrasomy and pentasomy. Pediatrics 96:672-82
Bender, B G; Harmon, R J; Linden, M G et al. (1995) Psychosocial adaptation of 39 adolescents with sex chromosome abnormalities. Pediatrics 96:302-8

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