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12 Possible Causes for Arthralgia, Hyperlipidemia Type 5, Progressive Polyneuropathy

  • Multiple Myeloma

    […] to multiple myeloma The initial presentation occasionally is a polyneuropathy when it is part of a POEMS syndrome (mostly the sclerotic form).[radiopaedia.org] The most common symptoms are joint pain (arthralgia), pain and numbness in the fingers and toes in response to cold (Raynaud’s phenomenon), weakness, and purpura.[rarediseases.org] Symptoms include fever, chills, arthralgia, myalgia, facial flushing, facial edema, vomiting, weakness, shortness of breath, hypotension, syncope, chest tightness, or angina[investors.amgen.com]

  • Waldenstrom Macroglobulinemia

    A 68-year-old woman consulted for new-onset oedemas, arthralgias and purpuric lesions in lower limbs.[revistanefrologia.com] Neuropathy is typically slowly progressive, distal, symmetrical, and sensorimotor.[emedicine.medscape.com] […] patients with WM, accompanied by occasional fever, night sweats, and weight loss. 1 Patients may also develop Schnitzler’s syndrome, a term to describe skin lesions, fever, and arthralgia[academic.oup.com]

  • Diabetes Mellitus

    There have been postmarketing reports of severe and disabling arthralgia in patients taking DPP-4 inhibitors.[mrknewsroom.com]

  • Scleredema Adultorum

    710.1 Excludes circumscribed scleroderma ( 701.0 ) Applies To Acrosclerosis CRST syndrome Progressive systemic sclerosis Scleroderma Use Additional Use additional code to[icd9data.com] Up to 9% of these patients can have arthralgias. [6] Unlike SSc, however, digital ulceration, nail fold capillary changes, Raynaud's phenomenon, resorption of phalanges, and[indianjrheumatol.com] She had recently been diagnosed with type 2 diabetes mellitus with a HgbA1c of 7. 5%. She has hypertension, hyperlipidemia, and depression.[ijcasereportsandimages.com]

  • Autosomal Dominant Myoglobinuria

    polyneuropathy type SLC25A19 Thyrotoxic periodic paralysis type 1 CACNA1S Thyrotoxic periodic paralysis type 2 KCNJ18 Tibial muscular dystrophy, tardive TTN Tourette syndrome[centogene.com] […] nephropathy (consider renal biopsy) Sinus issues : granulomatosis with polyangiitis (“Wegener’s granulomatosis”) Lung issues : Goodpasture syndrome Child with: abdominal pain, arthralgias[medicalmediareview.com] 2 Diabetes LPL Lipoprotein Lipase Familial Combined Hyperlipidemia (FCHL) Lipoprotein Lipase Deficiency LRP5 Low Density Lipoprotein Receptor-Related Protein 5 Congenital[bcm.edu]

  • Glutamate Formiminotransferase Deficiency

    […] characterized by severe motor retardation and progressive scoliosis.[amp.pharm.mssm.edu] […] due to hepatic triglyceride lipase deficiency Hyperlipidemia type 3 Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 3 Hyperlipoproteinemia type 4 Hyperlipoproteinemia[csbg.cnb.csic.es] […] term) and is characterized by recurrent episodes of urticaria-like skin rash triggered by exposure to cold associated with low-grade fever, general malaise, eye redness and arthralgia[amp.pharm.mssm.edu]

  • Anonychia Congenita Totalis

    polyneuropathy type), 613710 TPK1 Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type), 614458 SLC19A2 Thiamine-responsive megaloblastic anemia syndrome[gsdseq.ir] Thickened skin Type I diabetes mellitus Absent eyebrow Autoimmune hemolytic anemia Myositis Thrombocytosis Severe combined immunodeficiency Lymphopenia Pain Fever Arthritis Arthralgia[mendelian.co] […] due to hepatic triglyceride lipase deficiency Hyperlipidemia type 3 Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 3 Hyperlipoproteinemia type 4 Hyperlipoproteinemia[csbg.cnb.csic.es]

  • Marfanoid Habitus with Situs Inversus

    Sx: dark connective tissue, brown pigmented sclera, uring turns black on standing, may have arthralgias (homogentistic acid toxic to cartilage AR tyrosinase defect or defective[quizlet.com] […] leg weakness that ascends (following GI/URI infection) Guillain-Barre syndrome (autoimmune acute inflammatory demylenating polyneuropathy) -R.[studyblue.com] High LDL levels with severe arherosclersis and tendon xanthomas Familial hyperlipidemia type IIA AD defect in LDL receptors on chromosome 19 (homo LDL of 700 with MI before[cram.com]

  • Eye Defects - Arachnodactyly - Cardiopathy Syndrome

    […] myoclonic epilepsy with dystonia Progressive non-fluent aphasia Progressive polyneuropathy with bilateral striatal necrosis Progressive supranuclear palsy Progressive supranuclear[se-atlas.de] […] for 3/12 in four or more joints Minor criteria Current/historic Brighton score of 1, 2 or 3/9 (0, 1, 2, 3/9 if 50 years old) Arthralgia for minimum of 3 months in 1–3 joints[medical-dictionary.thefreedictionary.com] 2 Diabetes LPL Lipoprotein Lipase Familial Combined Hyperlipidemia (FCHL) Lipoprotein Lipase Deficiency LRP5 Low Density Lipoprotein Receptor-Related Protein 5 Congenital[bcm.edu]

  • 3Beta-Hydroxy-Delta5-C27-Steroid Oxidoreductase Deficiency

    peripheral neuropathy Limited extraocular movements Internuclear ophthalmoplegia Global developmental delay Hypertelorism Strabismus Cataract Visual impairment Wide nasal[mendelian.co] […] due to hepatic triglyceride lipase deficiency Hyperlipidemia type 3 Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 3 Hyperlipoproteinemia type 4 Hyperlipoproteinemia[csbg.cnb.csic.es] Phenotype % cases Hepatomegaly Uncommon - Between 30% and 50% cases Polyneuropathy Uncommon - Between 30% and 50% cases Malabsorption Uncommon - Between 30% and 50% cases Arthralgia[mendelian.co]

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