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Results 1 - 10 of 15 for History of neonatal hypotonia
  1. 5q31.3 microdeletion syndrome 
    ... early fetal development. Affected people typically have no history of the disorder in their family. Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion ...
    https://medlineplus.gov/.../condition/5q313-microdeletion-syndrome - Genetics
  2. PURA syndrome 
    ... development. These cases occur in people with no history of the disorder in their family. PURA-related neurodevelopmental disorder PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Genetic Testing Registry: PURA-related ...
    https://medlineplus.gov/genetics/condition/pura-syndrome - Genetics
  3. Lowe syndrome 
    ... affected children have weak muscle tone from birth (neonatal hypotonia), which can contribute to feeding difficulties, problems with ... the gene and occur in males with no history of the disorder in their family.Females who ...
    https://medlineplus.gov/genetics/condition/lowe-syndrome - Genetics
  4. Kearns-Sayre Syndrome From the National Institutes of Health (National Center for Advancing Translational Sciences)  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Eye Diseases/Specifics ... Eye Diseases ... National Center for Advancing Translational Sciences ... From the ...
    https://rarediseases.info.nih.gov/.../6817/kearns-sayre-syndrome - External Health Links
  5. What Are Related Conditions? (Marfan Foundation)  
    Marfan Syndrome/Related Issues ... Marfan Syndrome ... Marfan Foundation ... The Marfan Foundation's mission is to save lives and improve the quality of life of individuals ...
    https://marfan.org/conditions - External Health Links
  6. MECP2-related severe neonatal encephalopathy 
    ... the gene and occur in people with no history of the disorder in their family. Methyl-cytosine ...
    https://medlineplus.gov/...p2-related-severe-neonatal-encephalopathy - Genetics
  7. 6q24-related transient neonatal diabetes mellitus 
    ... early embryonic development. Affected people typically have no history of the disorder in their family.Sometimes, the ...
    https://medlineplus.gov/...ated-transient-neonatal-diabetes-mellitus - Genetics
  8. Sialuria 
    ... cases have occurred in people with no known history of the disorder in their family. These cases ...
    https://medlineplus.gov/genetics/condition/sialuria - Genetics
  9. Canavan disease 
    ... J, Wang DJ, Bilaniuk L, Leone P. Natural history of Canavan disease revealed by proton magnetic resonance ...
    https://medlineplus.gov/genetics/condition/canavan-disease - Genetics
  10. 2-hydroxyglutaric aciduria 
    ... IDH2 gene and occurs in people with no history of the condition in their family. 2-HGA ...
    https://medlineplus.gov/.../condition/2-hydroxyglutaric-aciduria - Genetics
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