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Fragile X syndrome in Democratic Republic of Congo: dysmorphic, cognitive and behavioral findings in 14 subjects from three families.
Kasole Lubala, Toni; Kayembe-Kitenge, Tony; Lubala, Nina; Kanteng, Gray; Luboya, Oscar; Hagerman, Randi; Lukusa-Tshilobo, Prosper; Lumaka, Aimé.
Afiliação
  • Kasole Lubala T; Division of Dysmorphology & Birth Defects, Department of Pediatrics, University of Lubumbashi, Congo.
  • Kayembe-Kitenge T; Higher Institute of Medical Techniques, Lubumbashi.
  • Lubala N; Toxicology and environment unit, University of Lubumbashi, DR Congo.
  • Kanteng G; Division of Dysmorphology & Birth Defects, Department of Pediatrics, University of Lubumbashi, Congo.
  • Luboya O; Division of Dysmorphology & Birth Defects, Department of Pediatrics, University of Lubumbashi, Congo.
  • Hagerman R; Division of Dysmorphology & Birth Defects, Department of Pediatrics, University of Lubumbashi, Congo.
  • Lukusa-Tshilobo P; Higher Institute of Medical Techniques, Lubumbashi.
  • Lumaka A; Department of Pediatrics, University of California Davis Medical Center, Sacramento, CA, USA.
Clin Dysmorphol ; 33(1): 9-15, 2024 Jan 01.
Article em En | MEDLINE | ID: mdl-38038060
ABSTRACT
This study reports on 14 individuals with Fragile X syndrome from 3 Congolese Families. The majority (8/14) were males, with an average age of 18.4 (±11.1 [14-38]) years old. Typical dysmorphic characteristics of Fragile-X syndrome including elongated face, large and prominent ears were found in both males and females with the full mutation. Macroorchidism was found in all post-pubertal boys. The cognitive ability in our cohort varies widely ranging from mild (IQ 50-70) to moderate (IQ 35-49) intellectual disability (Average IQ of 60). All our female patients have ID.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Limite: Adolescent / Adult / Female / Humans / Male País como assunto: Africa Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Limite: Adolescent / Adult / Female / Humans / Male País como assunto: Africa Idioma: En Ano de publicação: 2024 Tipo de documento: Article