Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 26 for Distal amyotrophy
Did you mean Distal amyotrophic?
  1. Distal hereditary motor neuropathy, type V 
    ... type 5 Distal hereditary motor neuronopathy, type V Distal spinal muscular atrophy, type V DSMAV HMN V Spinal muscular atrophy, ... in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. Am J Hum Genet. 2003 May; ...
    https://medlineplus.gov/...distal-hereditary-motor-neuropathy-type-v - Genetics
  2. Spinal muscular atrophy with respiratory distress type 1 
    ... signs and symptoms of the condition. Autosomal recessive distal spinal muscular atrophy 1 DHMN6 Diaphragmatic spinal muscular atrophy Distal hereditary ...
    https://medlineplus.gov/...-atrophy-with-respiratory-distress-type-1 - Genetics
  3. Distal hereditary motor neuropathy, type II 
    Distal hereditary motor neuropathy, type II is a progressive disorder that affects nerve cells in the spinal cord. It results in muscle weakness and affects ...
    https://medlineplus.gov/...istal-hereditary-motor-neuropathy-type-ii - Genetics
  4. Spinal muscular atrophy with progressive myoclonic epilepsy 
    ... symptoms of the condition. Hereditary myoclonus with progressive distal muscular atrophy Jankovic-Rivera syndrome SMA-PME SMAPME Genetic Testing ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
  5. Troyer syndrome 
    ... paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties ( ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  6. TRPV4 gene 
    ... includes Charcot-Marie-Tooth disease type 2C, congenital distal spinal muscular atrophy, which is characterized by weakness of muscles in ... PubMed BRACHYOLMIA TYPE 3; BCYM3 ... SPINAL MUSCULAR ATROPHY; SPSMA TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY V, ...
    https://medlineplus.gov/genetics/gene/trpv4 - Genetics
  7. GARS1 gene 
    ... in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. Am J Hum Genet. 2003 May; ...
    https://medlineplus.gov/genetics/gene/gars1 - Genetics
  8. IGHMBP2 gene 
    ... U, Schuetz A, Schuelke M. Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 ...
    https://medlineplus.gov/genetics/gene/ighmbp2 - Genetics
  9. DCTN1 gene 
    ... Finnegan K, Holzbaur EL, Fischbeck KH, Ludlow CL. Distal spinal and bulbar muscular atrophy caused by dynactin mutation. Ann Neurol. 2005 May; ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  10. Describing SMA (Cure SMA)  
    Spinal Muscular Atrophy/Start Here ... Spinal Muscular Atrophy ... Cure SMA ... Make today a breakthrough. No two people with spinal muscular atrophy (SMA) have identical ...
    https://www.curesma.org/describing-sma - External Health Links
previous · 1 · 2 · 3 · next