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Results 1 - 10 of 22 for Diaphragm disorder
  1. Microphthalmia with linear skin defects syndrome 
    ... separates the abdomen from the chest cavity (the diaphragm), which is called a diaphragmatic hernia, may occur in people with this disorder. Affected individuals may also have short stature and ...
    https://medlineplus.gov/...thalmia-with-linear-skin-defects-syndrome - Genetics
  2. Myasthenia gravis 
    ... separates the abdomen from the chest cavity (the diaphragm) can cause breathing problems in some people with myasthenia gravis. About 10 percent of people with this disorder experience a potentially life-threatening complication in which ...
    https://medlineplus.gov/genetics/condition/myasthenia-gravis - Genetics
  3. NPHS2 gene 
    ... of normal slit diaphragms. Without a functional slit diaphragm, molecules pass through the kidneys abnormally and are excreted in urine. The filtering ability of the kidneys worsens from birth, eventually leading to end-stage renal disease. More About This Health Condition NPHS2 gene mutations ...
    https://medlineplus.gov/genetics/gene/nphs2 - Genetics
  4. Spinal muscular atrophy with respiratory distress type 1 
    ... inhalation to allow the lungs to expand. With diaphragm paralysis, affected ... of the disorder later in childhood.Soon after respiratory failure occurs, ...
    https://medlineplus.gov/...-atrophy-with-respiratory-distress-type-1 - Genetics
  5. NPHS1 gene 
    ... of normal slit diaphragms. Without a functional slit diaphragm, molecules pass through the kidneys abnormally and are excreted in urine. The filtering ability of the kidneys worsens from birth, eventually leading to end-stage renal disease. More About This Health Condition CNF nephrin nephrin ...
    https://medlineplus.gov/genetics/gene/nphs1 - Genetics
  6. Congenital nephrotic syndrome 
    ... of normal slit diaphragms. Without a functional slit diaphragm, more molecules pass ... renal disease.NPHS1 gene mutations cause all cases of congenital ...
    https://medlineplus.gov/.../condition/congenital-nephrotic-syndrome - Genetics
  7. Pallister-Killian mosaic syndrome 
    ... separates the abdomen from the chest cavity (the diaphragm). This potentially ... this disorder have severe to profound intellectual disability and other ...
    https://medlineplus.gov/.../pallister-killian-mosaic-syndrome - Genetics
  8. White-Sutton syndrome 
    ... separates the abdomen from the chest cavity (the diaphragm), which is called a diaphragmatic hernia. ... autism spectrum disorder, or both. However, most of these affected individuals ...
    https://medlineplus.gov/genetics/condition/white-sutton-syndrome - Genetics
  9. Congenital diaphragmatic hernia 
    ... of the diaphragm, or those in which the diaphragm muscle is absent with only a thin membrane in its place, ... the condition appears as a feature of a disorder that affects many body systems, called a syndrome. ...
    https://medlineplus.gov/.../congenital-diaphragmatic-hernia - Genetics
  10. Fryns syndrome 
    ... with the signs and symptoms of several other disorders. These factors can make Fryns syndrome difficult to diagnose.Most people with Fryns syndrome have a defect in the muscle that separates the abdomen from the chest cavity (the diaphragm). The most common defect is a congenital diaphragmatic ...
    https://medlineplus.gov/genetics/condition/fryns-syndrome - Genetics
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