Neuroaxonal dystrophy renal tubular acidosis

Genetic and Rare Diseases Information Center (GARD)

Maccario Mena Weir syndrome
CNS disorder characterized by severe behavioral retardation, hypotonia, inability to talk, marked tremors, gait disturbances and inability to concentr

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Neuroaxonal dystrophy renal tubular acidosis
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Questions & Answers (Found: 0 Resources)

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More Information (Found: 1 Resources)
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- General
  - PubMed lists journal articles that discuss Neuroaxonal dystrophy renal tubular acidosis. Click on the link to go to PubMed and review citations to these articles.
Support Groups (Found: 4 Resources)
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- Umbrella Organizations
  - Genetic Alliance
    4301 Connecticut Avenue NW
    Suite 404
    Washington, DC 20008-2369
    Telephone: 202-966-5557
    Fax: 202-966-8553
    E-mail: info@geneticalliance.org
    Web site: http://www.geneticalliance.org
    
    National Organization for Rare Disorders (NORD)
    55 Kenosia Avenue
    PO Box 1968
    Danbury, CT 06813-1968
    Toll-free: 1-800-999-6673 (voicemail only)
    Telephone: 203-744-0100
    TTY: 203-797-9590
    Fax: 203-798-2291
    E-mail: orphan@rarediseases.org
    Web site: http://www.rarediseases.org/
- Live Chat
  - The National Organization of Rare Disorders (NORD) has partnered with Inspire.com to launch an online community for people with rare diseases called The NORD Rare Disease Community. This community connects medical patients, family members, caregivers, and professionals. Click on The NORD Rare Disease Community to learn more.
    
    RareShare is an online social hub dedicated to patients, families and healthcare professionals affected by rare medical disorders. Click on RareShare to learn more.
More Search Tools (Found: 1 Resources)
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- - The NLM Gateway allows users to search across multiple resources offered on the National Library of Medicine's Web site. Some of these resources may be duplicated in the list of links above. Click on the link to go to the NLM Gateway, and search by condition name.

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