Three siblings with Woodhouse-Sakati syndrome in an Indian family

Clinical Dysmorphology

Volumn 17, Issue 1, 2008, Pages 57-60

  Koshy, George ^a   Danda, Sumita ^a   Thomas, Nihal ^a   Mathews, Vikram ^a   Viswanathan, Vijay ^b  

^a CHRISTIAN MEDICAL COLLEGE   (India)

^b MV Hospital for Diabetes   (India)

Author keywords

India; Thrombocytopenia; Woodhouse Sakati

Indexed keywords

ANTIDIABETIC AGENT; GLUCOSE; INSULIN;

ADULT; ALOPECIA; ARTICLE; CAMPTODACTYLY; CASE REPORT; DIABETES MELLITUS; FEMALE; GENETIC DISORDER; GLUCOSE BLOOD LEVEL; GLUCOSE TOLERANCE; HEARING LOSS; HUMAN; HYPERGONADOTROPIC HYPOGONADISM; HYPOGONADOTROPIC HYPOGONADISM; IDIOPATHIC THROMBOCYTOPENIC PURPURA; IMMUNOPHENOTYPING; MENSTRUATION; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SIBLING; ULTRASOUND; VAGINAL DELIVERY; WOODHOUSE SAKATI SYNDROME;

ADULT; ALOPECIA; DEAFNESS; DIABETES MELLITUS; ELECTROCARDIOGRAPHY; HUMANS; INDIA; MENTAL RETARDATION; PHENOTYPE; PURPURA, THROMBOCYTOPENIC, IDIOPATHIC; SIBLINGS; SYNDROME;

EID: 40349100155     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e3282beb59e     Document Type: Article

References (4)

1. Al-Swailem SA, Al-Assiri AA, Al-Torbak AA (2006). Woodhouse Sakati syndrome associated with bilateral keratoconus. Br J Ophthalmol 90:116-117.
2. Gul D, Ozata M, Mergen H, Odabasi Z, Mergen M (2000). Woodhouse and Sakati Syndrome (MIM 241080): report of a new patient. Clin Dysmorphol 9:123-125.
3. Oerter KE, Friedman TC, Anderson HC, Casserole FG (1992). Familial syndrome of endocrine and neuroectodermal abnormalities. Am J Med Genet 44:487-491.
4. Woodhouse NJY, Sakati NA (1983). A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation deafness and ECG abnormalities. J Med Genet 20:216-219.