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Tremor is a major feature of 9p13 deletion syndrome.
Ferreira, Susana Isabel; Cinnirella, Giacomo; Ramos, Lina; Suppa, Antonio; Pires, Luís Miguel; Nardone, Anna Maria; Camerota, Letizia; Lanciotti, Silvia; Galasso, Cinzia; De Maio, Fernando; de Melo, Joana Barbosa; Carreira, Isabel Marques; Brancati, Francesco.
Afiliação
  • Ferreira SI; Laboratory of Cytogenetics and Genomics, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
  • Cinnirella G; Medical Genetics Residency Program, Tor Vergata University of Rome and University of L'Aquila, L'Aquila, Italy.
  • Ramos L; Medical Genetics Unit, Pediatric Hospital, Coimbra Hospital and University Centre, Coimbra, Portugal.
  • Suppa A; Department of Human Neurosciences, Sapienza University, Rome, Italy.
  • Pires LM; Neuromed IRCCS, Pozzilli, Isernia, Italy.
  • Nardone AM; Laboratory of Cytogenetics and Genomics, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
  • Camerota L; Laboratory of Medical Genetics, Policlinico Tor Vergata, Rome, Italy.
  • Lanciotti S; Medical Genetics Residency Program, Tor Vergata University of Rome and University of L'Aquila, L'Aquila, Italy.
  • Galasso C; Medical Genetics Residency Program, Tor Vergata University of Rome and University of L'Aquila, L'Aquila, Italy.
  • De Maio F; Department of Systems Medicine, Division of Child Neurology and Psychiatry, Tor Vergata University of Rome, Rome, Italy.
  • de Melo JB; Department of Orthopaedic Surgery, Tor Vergata University of Rome, Rome, Italy.
  • Carreira IM; Laboratory of Cytogenetics and Genomics, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
  • Brancati F; Coimbra Institute for Clinical and Biomedical Research (iCBR), Area of Environment, Genetics and Oncobiology (CIMAGO), Faculty of Medicine, University of Coimbra, Center for Innovative Biomedicine and Biotechnology (CIBB), Coimbra, Portugal.
Am J Med Genet A ; 182(11): 2694-2698, 2020 11.
Article em En | MEDLINE | ID: mdl-32896075
Proximal interstitial deletions of chromosome 9p13 have been described only in a few patients with developmental delay, moderate intellectual disability, craniofacial dysmorphism, short stature, genital anomalies, and precocious puberty. To corroborate and expand these findings, we report on two novel syndromic male patients with 9p13 deletions suffering from a similar form of tremor and compare them with literature data. Despite genomic variability in deletion sizes, all patients displayed homogeneous dysmorphism and clinical manifestations, including very invalidating tremor. Furthermore, we outlined a region of around 2 Mb shared in common by all patients with nearly 70 genes, among which NPR2 might have a role in the phenotype. These data delineate interstitial 9p13 deletion syndrome with tremor as a major feature.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Tremor / Anormalidades Múltiplas / Cromossomos Humanos Par 9 / Deleção Cromossômica Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Tremor / Anormalidades Múltiplas / Cromossomos Humanos Par 9 / Deleção Cromossômica Idioma: En Ano de publicação: 2020 Tipo de documento: Article