Lenticular Opacities in Carriers of Lowe's Syndrome

Ophthalmology

Volumn 93, Issue 8, 1986, Pages 1041-1045

  Cibis, Gerhard W ^a,b   Waeltermann, Joanne M ^a   Whitcraft, Chauncey T ^b   Tripathi, Ramesh C ^c   Harris, David J ^a  

^a CHILDREN S MERCY HOSPITAL   (United States)

^b UNIVERSITY OF KANSAS   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

Author keywords

carrier state; cataracts; genetic counseling; Lowe's syndrome; Lyon hypothesis; X linked recessive inheritance

Indexed keywords

CARRIER; CATARACT; CENTRAL NERVOUS SYSTEM; CLINICAL ARTICLE; DIAGNOSIS; ETIOLOGY; GENETIC COUNSELING; HEREDITY; HETEROZYGOTE DETECTION; HUMAN; KIDNEY; LOWE SYNDROME; LYON HYPOTHESIS; PEDIGREE; PRIORITY JOURNAL; VISUAL SYSTEM; X CHROMOSOME RECESSIVE INHERITANCE;

EID: 0022470464     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(86)33623-6     Document Type: Article

References (7)

1. Sex chromatin and gene action in the mammalian X-chromosome
2. Lowe syndrome: identification of the carrier state
3. Lowe's syndrome
4. Corneal keloid in Lowe's syndrome
5. Lowe's Syndrome
6. Presenile cataract formation and decreased activity of galactosemic enzymes
7. The effect of diabetes mellitus and diabetic therapy on cataract formation