Woodhouse Sakati syndrome associated with bilateral keratoconus [3]

British Journal of Ophthalmology

Volumn 90, Issue 1, 2006, Pages 116-117

  Al Swailem, Samar A ^a   Al Assiri, A A ^a   Al Torbak, A A ^a  

^a KING KHALED EYE SPECIALIST HOSPITAL   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AMENORRHEA; CASE REPORT; CLINICAL FEATURE; DETERIORATION; DISEASE ASSOCIATION; ECG ABNORMALITY; FEMALE; HUMAN; HYPOGONADISM; HYPOTHYROIDISM; KERATOCONUS; KERATOMETRY; LETTER; PENETRATING KERATOPLASTY; PRIORITY JOURNAL; SLIT LAMP; SYSTEMIC DISEASE; VISUAL ACUITY; VISUAL IMPAIRMENT; WOODHOUSE SAKATI SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; FEMALE; HUMANS; HYPOGONADISM; KERATOCONUS; SYNDROME; VISION DISORDERS;

EID: 29744447993     PISSN: 00071161     EISSN: None     Source Type: Journal    
DOI: 10.1136/bjo.2005.080101     Document Type: Letter

References (6)

1. Rabinowitz YS. Keratoconus. Surv Ophthalmol 1998;42:297-319.
2. Tyynismaa H, Sistonen P, Tuupanen S, et al. A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. Invest Ophthalmol Vis Sci 2002;43:3160-4.
3. Adachi W, Mitsuishi Y, Terai K, et al. The association of HLA with young-onset keratoconus in Japan. Am J Ophthalmol 2002;133:557-9.
4. Woodhouse NJ, Sakati NA. A syndrome of hypogonadisim, alopecia, diabetes mellitus, mental retardation, deafness and ECG abnormalities. J Med Genet 1983;20:216-19.
5. Gul D, Ozata M, Mergen H, et al. Woodhouse and Sakati syndrome (MIM 241080) report of a new patient. Clin Dysmorph 2000;9:123-5.
6. Morrison DA, Rosser EM, Claoue C. Keratoconus associated with a chromosome 7, 11 translocation. Eye 2001;15:556-7.