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Increased intracranial pressure in a patient with Congenital Heart Defect and Ectodermal Dysplasia (CHDED): Extension of phenotype and review of literature.
Alghaith, Fahad A; Arts, Heleen H; Plourde, Francois J; Boswall, Andrew; Gulati, Partima; McNeely, P Daniel; Acott, Philip D; Wong, Kenny K; Dyack, Sarah.
Affiliation
  • Alghaith FA; Division of Clinical Genomics, Department of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Arts HH; Division of Clinical Genomics, Department of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Plourde FJ; Division of Medical Genetics, Maritime Medical Genetics Service, IWK Health Centre, Nova Scotia, Canada.
  • Boswall A; Department of Ophthalmology and Visual Sciences, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Gulati P; Division of Neurology, Department of Pediatrics and Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
  • McNeely PD; Division of Neurosurgery, Department of Surgery, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Acott PD; Division of Nephrology, Department of Surgery, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Wong KK; Division of Cardiology, Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Dyack S; Division of Medical Genetics, Department of Pediatrics and Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Am J Med Genet A ; 191(2): 554-558, 2023 02.
Article in En | MEDLINE | ID: mdl-36308391
ABSTRACT
Congenital heart defect (CHD) is a birth defect that affects the structure of the heart. Although CHD is often multifactorial, it can also be inherited as part of a Mendelian disorder such as in congenital heart defect and ectodermal dysplasia (CHDED). This disorder is caused by de novo variants in PRKD1. Here, we describe a patient with a novel de novo variant of PRKD1 with phenotypic features consistent with CHDED. Previously unreported features were noted including high intracranial pressure (ICP), partial anomalous pulmonary venous return (PAPVR), and bifid uvula. We suggest that these features may be associated with CHDED.
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Full text: 1 Database: MEDLINE Main subject: Ectodermal Dysplasia / Cleft Palate / Heart Defects, Congenital Limits: Humans Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Ectodermal Dysplasia / Cleft Palate / Heart Defects, Congenital Limits: Humans Language: En Year: 2023 Type: Article