COL4A1 and Intraventricular Hemorrhage

Authors

  • Laura Leite de Almeida Serviço de Pediatria. Centro Hospitalar Universitário de São João. Porto; Faculdade de Medicina. Universidade do Porto. Porto.
  • Ana Grangeia Faculdade de Medicina. Universidade do Porto. Porto; Serviço de Genética Médica. Centro Hospitalar Universitário de São João. Porto.
  • Luísa Sampaio Faculdade de Medicina. Universidade do Porto. Porto; Serviço de Neurorradiologia. Centro Hospitalar Universitário de São João. Porto.
  • Ana Vilan Faculdade de Medicina. Universidade do Porto. Porto; Serviço de Neonatologia. Centro Hospitalar Universitário de São João. Porto.

DOI:

https://doi.org/10.20344/amp.20515

Keywords:

Cerebral Hemorrhage/genetics, Collagen Type IV/genetics, Fetal Diseases/genetics, Infant, Newborn

Abstract

N/a.

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References

Lanfranconi S, Markus HS. COL4A1 mutations as a monogenic cause of cerebral small vessel disease: a systematic review. Stroke. 2010;41:e513-8.

Plaisier E, Ronco P. COL4A1-related disorders. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJ, Gripp KW, et al, editors. GeneReviews®. Seattle: University of Washington; 2009.

Vahedi K, Alamowitch S. Clinical spectrum of type IV collagen (COL4A1) mutations: a novel genetic multisystem disease. Curr Opin Neurol. 2011;24:63-8.

In Press

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Published

2024-05-29

How to Cite

1.
Leite de Almeida L, Grangeia A, Sampaio L, Vilan A. COL4A1 and Intraventricular Hemorrhage. Acta Med Port [Internet]. 2024 May 29 [cited 2024 Jun. 28];. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/20515

Issue

In Press

Section

Medical Image

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