National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Woods Black Norbury syndrome



Other Names:
Neonatal death immune deficiency; X-linked immunoneurological disorder
Categories:

The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
orphanet

Orpha Number: 2571

Definition
X-linked immunoneurologic disorder is characterized by immune deficiency and neurological disorders in females, and by neonatal death in males.

Epidemiology
The syndrome has been described in only one family with nine affected individuals (five males and four females) spanning two generations.

Clinical description
Symptomatic females present slowly progressive proximal muscle weakness, leg hyperreflexia, pes cavus, increased muscle tone in the legs, poor bladder function, static reduced night vision, and frequent sinopulmonary infections associated with IgG2 deficiency. Males present with low birth weight and severe hypotonia that leads to death in the neonatal period.

Etiology
The gene locus has been mapped to Xq26-qter.

Differential diagnosis
The syndrome should be considered in the differential diagnosis of hereditary spastic paraplegia in females and of other causes of severe neonatal hypotonia in males.

Genetic counseling
The condition is thought to be transmitted in an X-linked dominant manner.

Visit the Orphanet disease page for more resources.
Last updated: 8/1/2009

This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.

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Medical Terms Other Names
Learn More:
HPO ID
30%-79% of people have these symptoms
Decreased circulating IgG2 level 0008348
Functional abnormality of the bladder 0000009
Hemiplegia/hemiparesis
Paralysis or weakness of one side of body
0004374
Hyperreflexia
Increased reflexes
0001347
Hypertonia 0001276
Nyctalopia
Night blindness
Night-blindness
Poor night vision
[ more ]
0000662
Nystagmus
Involuntary, rapid, rhythmic eye movements
0000639
Recurrent respiratory infections
Frequent respiratory infections
Multiple respiratory infections
respiratory infections, recurrent
Susceptibility to respiratory infections
[ more ]
0002205
5%-29% of people have these symptoms
Abnormal pleura morphology 0002103
Cataract
Clouding of the lens of the eye
Cloudy lens
[ more ]
0000518
Myopathy
Muscle tissue disease
0003198
Percent of people who have these symptoms is not available through HPO
Brisk reflexes 0001348
Neonatal death
Neonatal lethal
0003811
Neonatal hypotonia
Low muscle tone, in neonatal onset
0001319
Progressive proximal muscle weakness 0009073
Small for gestational age
Birth weight less than 10th percentile
Low birth weight
[ more ]
0001518
Spastic paraplegia 0001258
X-linked dominant inheritance 0001423
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Last updated: 7/1/2020

If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.

If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.

You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.

Healthcare Resources


Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.

Clinical Research Resources

  • The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.

These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

In-Depth Information

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Woods Black Norbury syndrome. Click on the link to view a sample search on this topic.

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