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97 Possible Causes for Cyanosis, primarily in the legs, severe muscle wasting

Did you mean: Cyanosis, primarily in the legs, severe, muscle wasting

  • Spinal Muscular Atrophy

    […] diagnosis of infants with congenital contractures and severe muscle weakness by wasting mainly confined to the upper limbs.[ncbi.nlm.nih.gov] The condition primarily affects the muscles that control chewing and swallowing, chest wall muscles, and arm and leg muscles.[ucsfbenioffchildrens.org] Neuromyopathy associated ketosis should be considered in all patients with severe muscle wasting presenting with an elevated anion gap metabolic ketoacidosis.[ncbi.nlm.nih.gov]

  • Spinal Muscular Atrophy Type 1

    This form affects primarily the muscles in the legs.[mda.org] atrophy type 1 with paradoxical breathing were placed on high-span PIP PEEP when sleeping from the point of diagnosis of spinal muscular atrophy.[ncbi.nlm.nih.gov] Three children with spinal muscular atrophy type 1 underwent multiple intrathecal and intravenous infusions of mesenchymal stem cells.[ncbi.nlm.nih.gov]

  • Pulmonary Embolism

    Deep veins are veins that exist deep within the body, primarily in the arms, shoulder, legs, pelvis, and neck.[curlie.org] […] blood clot which has originated in a vein of the leg or pelvis and traveled to the lungs and that is marked by labored breathing, chest pain, fainting, rapid heart rate, cyanosis[merriam-webster.com] CASE PRESENTATION: A nine-year-old female with spinal muscular atrophy type 1, chronic respiratory failure with tracheostomy and ventilator dependence presented with tachypnea[ncbi.nlm.nih.gov]

  • Distal Spinal Muscular Atrophy Type 3

    At 6 months, he had acute onset respiratory distress and cyanosis requiring intubation and ventilation.[annalsofian.org] Characterised by severe muscle wasting as in SMA type I accompanied by congenital bone fractures PCH Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH) Pontocerebellar[ipfs.io] This form affects primarily the muscles in the legs.[mda.org]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    This form affects primarily the muscles in the legs.[mda.org] At 6 months, he had acute onset respiratory distress and cyanosis requiring intubation and ventilation.[annalsofian.org] Characterised by severe muscle wasting as in SMA type I accompanied by congenital bone fractures PCH Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH) Pontocerebellar[ipfs.io]

  • Monomelic Amyotrophy

    Symptoms of increased sweating, coldness and cyanosis have been observed in a few patients.[ncbi.nlm.nih.gov] Rev Neurol (Paris) 145: 163–8 Medline, Google Scholar Hirayama K ( 2000 ) Juvenile muscular atrophy of distal upper extremity (Hirayama Disease).[doi.org] Disorder progression tends to be slower in patients who are younger than 40 at onset, [ 8 ] [ 9 ] are mildly obese, [ 10 ] have disorder restricted primarily to one limb,[cinabrio.over-blog.es]

  • Peripheral Vascular Disease

    PAD primarily affects the legs, but can also damage arteries in the kidneys, abdomen, feet, ankles, pelvis, hips, buttocks and arms.[lamvascular.com] With time, a decreased blood supply produces ischemic changes that cause the skin to assume a purple-black color that is characteristic of cyanosis and gangrene.[medical-dictionary.thefreedictionary.com] It is primarily caused by the buildup of fatty plaque in the arteries, which is called atherosclerosis.[cdc.gov]

  • Syringomyelia

    This symptoms can leads to complications such as aspiration, cyanosis, stridor as well as apnea.[2].[explainmedicine.com] Syringomyelia is marked clinically by pain and paresthesia, followed by muscular atrophy of the hands and analgesia with thermoanesthesia of the hands and arms, but with the[medical-dictionary.thefreedictionary.com] Extension of the syrinx into the lumbar region and involvement of the legs.[patient.info]

  • Beriberi

    It affects primarily 0.5–1 kg sized birds such as the herring gull (Larus argentatus), common starling (Sturnus vulgaris) and common eider (Somateria mollissima).[en.wikipedia.org] The disease was characterized by circulatory shock and peripheral cyanosis. All patients had severe lactic acidosis, in 5 of them without hypoxaemia.[ncbi.nlm.nih.gov] Classically it is characterized by multiple neuritis, muscular atrophy, weakness, cardiovascular changes, and progressive edema. beriberi the name given to thiamin deficiency[medical-dictionary.thefreedictionary.com]

  • Friedreich Ataxia

    FRDA was first described in 1863 as a disease that is primarily early onset, associated with progressive limb and gait ataxia, absent tendon reflexes from the legs, axonal[doi.org] Passive exercises and warming for peripheral cyanosis and cold feet. Diabetes (if present) will usually require insulin.[patient.info] atrophy, Dr.[sciencedaily.com]

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