Polychromasia capsulare (multicolored capsule): Report of three families

Transactions of the American Ophthalmological Society

Volumn 103, Issue , 2005, Pages 93-97

  Traboulsi, Elias I ^a   Chung, Daniel ^a   Koors, John M ^b   Bronwyn Bateman, J ^c   Raab, Edward L ^c   Edward Wilson, M ^c   Spaeth, George L ^c  

^a LERNER RESEARCH INSTITUTE   (United States)

^b East Alabama Eye Clinic   (United States)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; EYE COLOR; FAMILY; FEMALE; HUMAN; ILLUMINATION; INHERITANCE; LABORATORY; LENS CAPSULE; MALE; MYOTONIC DYSTROPHY; OPHTHALMOLOGY; OPHTHALMOSCOPY; POLYCHROMASIA CAPSULARE; PRIORITY JOURNAL; SEROLOGY; SLIT LAMP; VISUAL ACUITY; WILSON DISEASE;

ADULT; AGED; CHILD; CHILD, PRESCHOOL; COLOR; FEMALE; GENES, DOMINANT; HUMANS; LENS CAPSULE, CRYSTALLINE; LENS DISEASES; MALE; MIDDLE AGED; OPHTHALMOSCOPY; PEDIGREE;

EID: 29944436686     PISSN: 15456110     EISSN: 15456110     Source Type: Journal    
DOI: None     Document Type: Article

References (2)

1. Knox D, Wolfe RL, Murdoch JL, et al. Hereditary tinted lenses in two families. In: Birth Defects Original Article Series. Vol V, No. 2. New York: Alan R. Liss; 1969:166.
2. Mir S, Wheatley HM, Maumenee Hussels IE, et al. A comparative study of the fibrillin microfibrillar system in the lens capsule of normal and Marfan syndrome patients. Invest Ophthalmol Vis Sci 1998;39:84-93.