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Abnormal bone mineral content and density in people with tetrasomy 18p.
Moreira, Alvaro; Das, Hrishikesh; Hasi-Zogaj, Minire; Soileau, Bridgette; Hill, Annice; Bruder, Jan M; Hale, Daniel E; Cody, Jannine D.
Afiliação
  • Moreira A; Department of Pediatrics, Division of Neonatology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
  • Das H; The Chromosome 18 Registry and Research Society, San Antonio, Texas.
  • Hasi-Zogaj M; Department of Pediatrics, Division of Neonatology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
  • Soileau B; Department of Pediatrics, Chromosome 18 Clinical Research Center, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
  • Hill A; Department of Pediatrics, Chromosome 18 Clinical Research Center, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
  • Bruder JM; Department of Pediatrics, Chromosome 18 Clinical Research Center, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
  • Hale DE; Department of Medicine, Division of Endocrinology, University of Texas Health-San Antonio, San Antonio, Texas.
  • Cody JD; The Chromosome 18 Registry and Research Society, San Antonio, Texas.
Am J Med Genet A ; 179(3): 417-422, 2019 03.
Article em En | MEDLINE | ID: mdl-30637922
Tetrasomy 18p is a rare chromosomal abnormality, resulting from an additional iso-chromosome composed of two copies of the short arm. It is characterized by craniofacial abnormalities, neuromuscular dysfunction, and developmental delay. The Chromosome 18 Clinical Research Center has established the largest cohort of individuals with this rare genetic condition. Here, we describe a case series of 21 individuals with tetrasomy 18p who have a previously unreported clinical finding: low bone mineral density. Most individuals met criteria for low bone density despite being relatively young (mean age of 21 years). Clinicians providing care to individuals affected by Tetrasomy 18p should be aware of their increased risk for decreased bone density and pathological fractures.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fenótipo / Densidade Óssea / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fenótipo / Densidade Óssea / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article