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A patient with Pitt-Hopkins syndrome with concomitant common variable immunodeficiency.
Malik, Shahzara; Jeanpierre, Latoya; Cianferoni, Antonella; Ruffner, Melanie; Sullivan, Kathleen E.
Afiliación
  • Malik S; College of Medicine and Health Sciences, Mohammed Bin Rashid University of Medicine and Health Sciences (MBRU), Dubai, United Arab Emirates.
  • Jeanpierre L; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Cianferoni A; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Ruffner M; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Sullivan KE; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Am J Med Genet A ; 194(4): e63490, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38066705
In patients with 18q deletion syndrome (18q-), immunodeficiency, autoimmunity, and allergies have been described in a subset. Pitt-Hopkins syndrome represents a specific subset of patients with 18q- who have a proximal deletion involving the TCF4 gene or a TCF4 variant. Immunodeficiency has been reported in the overall 18q- population; however, immunodeficiency with Pitt-Hopkins syndrome has not been highlighted. This case report details the immunologic evaluations and the associated infections seen in a young adult with Pitt-Hopkins syndrome to underscore the challenges of managing adults with a complex phenotype who develop frequent infections. This patient with Pitt-Hopkins syndrome ultimately fulfilled the diagnostic criteria for common variable immunodeficiency. Immunoglobulin replacement has led to a somewhat improved infection pattern, although she continues to have aspiration events leading to pneumonia. This case highlights the clinical evolution of Pitt-Hopkins syndrome and serves as a reminder that immunodeficiency can occur in this syndrome.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunodeficiencia Variable Común / Discapacidad Intelectual Límite: Female / Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunodeficiencia Variable Común / Discapacidad Intelectual Límite: Female / Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos
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