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Results 1 - 9 of 9 for Upper limb hypotonia
  1. Spastic paraplegia type 49 
    ... limbs, whereas the complex types also involve the upper limbs (to a lesser ... tone (hypotonia) that starts in infancy. During childhood, spasticity and ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-49 - Genetics
  2. CASK-related intellectual disability 
    ... between the nose and mouth (philtrum); a protruding upper jaw (maxilla); a short ... in the limbs. Movement problems such as involuntary tensing of various ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  3. Achondroplasia: About the Disease From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Dwarfism/Start Here ... Dwarfism ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information about ...
    https://rarediseases.info.nih.gov/diseases/8173/achondroplasia - External Health Links
  4. Dermatomyositis From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Myositis/Start Here ... Myositis ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information about ...
    https://rarediseases.info.nih.gov/diseases/6263/dermatomyositis - External Health Links
  5. Kearns-Sayre Syndrome From the National Institutes of Health (National Center for Advancing Translational Sciences)  
    Find symptoms and other information about Kearns-sayre syndrome. ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Eye Diseases/Specifics ... Eye Diseases
    https://rarediseases.info.nih.gov/.../6817/kearns-sayre-syndrome - External Health Links
  6. LAMA2-related muscular dystrophy 
    ... have severe muscle weakness, lack of muscle tone (hypotonia), little spontaneous movement, and joint deformities (contractures). Weakness ... of a group of muscle disorders classified as limb-girdle muscular ... of the shoulders, upper arms, pelvic area, and thighs. Children with late- ...
    https://medlineplus.gov/.../lama2-related-muscular-dystrophy - Genetics
  7. Fryns syndrome 
    ... in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype ...
    https://medlineplus.gov/genetics/condition/fryns-syndrome - Genetics
  8. Mitochondrial Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Muscle Disorders/Specifics ... Muscle Disorders ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Neuromuscular Disorders/Specifics ... Neuromuscular ...
    https://www.ninds.nih.gov/.../disorders/mitochondrial-disorders - External Health Links
  9. TUBB3 gene 
    ... condition lead to intellectual disability, weak muscle tone (hypotonia), and progressive muscle stiffness (spasticity) in affected individuals. ...
    https://medlineplus.gov/genetics/gene/tubb3 - Genetics