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brain small vessel disease 1 with or without ocular anomalies

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Any porencephaly in which the cause of the disease is a mutation in the COL4A1 gene.

Synonyms

  • ADT1P
  • BSVD
  • BSVD1
  • COL4A1 porencephaly
  • COL4A1-related brain small vessel disease with haemorrhage
  • COL4A1-related brain small vessel disease with hemorrhage
  • COL4A1-related familial vascular leukoencephalopathy
  • COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome
  • POREN1
  • T1P
  • autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy
  • brain small vessel disease with Axenfeld-Riegar anomaly
  • brain small vessel disease with axenfeld-rieger anomaly
  • brain small vessel disease with haemorrhage
  • brain small vessel disease with hemorrhage
  • brain small vessel disease with or without ocular anomalies
  • hemiplegia, infantile, with porencephaly
  • hemiplegia, infantile, with porencephaly porencephaly, type 1
  • infantile hemiparesis
  • leukoencephalopathy with axenfeld-rieger anomaly
  • porencephaly 1
  • porencephaly caused by mutation in COL4A1
  • porencephaly type 1
  • porencephaly, type 1, autosomal dominant
  • retinal arteriolar tortuosity, infantile hemiparesis, and leukoencephalopathy, autosomal dominant
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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