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402 Possible Causes for Autosomal Dominant, Tenosynovitis

  • Hypercholesterolemia

    RATIONALE: Autosomal-dominant hypercholesterolemia (ADH) is characterized by elevated low-density lipoprotein cholesterol levels and increased risk for coronary vascular disease[ncbi.nlm.nih.gov] Severe hypercholesterolemia associated or not with xanthomas in a child may suggest the diagnosis of homozygous autosomal dominant hypercholesterolemia (ADH), autosomal recessive[ncbi.nlm.nih.gov] Familial hypercholesterolemia (FH) is an inherited disorder of lipoprotein metabolism, transmitted in an autosomal dominant manner and clinically characterized by elevated[clinicaltrials.gov]

  • Familial Hypercholesterolemia

    Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol[ncbi.nlm.nih.gov] Abstract Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol[doi.org]

  • Amyloidosis

    dominant hereditary polyneuropathy related to the organ deposition of mutant forms of the transthyretin protein (encoded by mutated TTR ) over time.[nejm.org] BACKGROUND: Hereditary transthyretin amyloidosis is an autosomal dominant inherited disorder, first described in families with sensorimotor and autonomic neuropathy.[ncbi.nlm.nih.gov] The autosomal dominant transmission of HCM implies that many relatives are at risk for HCM associated morbidity and mortality, therefore genetic testing and counselling is[ncbi.nlm.nih.gov]

  • Gout

    We report 2 cases of familial juvenile hyperuricemic nephropathy, a rare autosomal dominant disorder characterized by uromodulin gene mutations leading to hyperuricemia secondary[ncbi.nlm.nih.gov] Extra-articular manifestations of gout can present in several ways, including tenosynovitis. We present a rare case of acute tibialis posterior gouty tenosynovitis.[ncbi.nlm.nih.gov] Genetic factors are believed to cause familial autosomal dominant CPPD chondrocalcinosis.[clevelandclinicmeded.com]

  • Hereditary Amyloidosis with Primary Renal Involement

    Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.[pnas.org] Fasciitis Pneumonia, Aspiration Psychosis Rotator Cuff (Impingement) Syndrome Somatization Disorder Thrombotic Thrombocytopenic Purpura Trigger Finger (Digital Stenosing Tenosynovitis[books.google.com] These diseases are inherited in an autosomal dominant manner with variable penetrance, and can present clinically at any time from the teen years to old age, though usually[ncbi.nlm.nih.gov]

  • Exostosis

    dominant manner?[orthobullets.com] Trigger finger is commonly secondary to stenosing tenosynovitis. Space occupying lesions in the tendon bed, although uncommon, may prevent smooth tendon gliding.[ncbi.nlm.nih.gov] Irrespective of origin, these two conditions can cause lameness (swinging leg) and carpal sheath tenosynovitis.[merckvetmanual.com]

  • Restless Legs Syndrome

    This is the third reported autosomal-dominant locus for RLS and the first autosomal-dominant RLS locus in the French-Canadian population.[ncbi.nlm.nih.gov] TENS Machine Video Analysis Yoga Helpful Products for Restless Leg Syndrome Call PhysioWorks Book Online Related Injuries Ankylosing Spondylitis Bunion Cramps de Quervain's Tenosynovitis[physioworks.com.au] This is the second RLS locus identified so far and the first consistent with an autosomal dominant inheritance pattern.[doi.org]

  • Rheumatoid Arthritis

    Hereditary angioedema (HAE) is a rare autosomal dominant condition characterized by recurrent attacks of edema at different locations of the body.[specialtypharmacytimes.com] The predominant clinical findings include palmar tenosynovitis, small joint synovitis, and carpal tunnel syndrome.[ncbi.nlm.nih.gov] Normal fat planes may be obliterated, which occurs as a result of joint effusion, edema, and tenosynovitis.[emedicine.medscape.com]

  • Systemic Amyloidosis

    dominant, hereditary systemic amyloidosis.[ncbi.nlm.nih.gov] The most common of the autosomal dominant systemic amyloidoses is caused by transthyretin variants.[doi.org] The familial type (ATTR type, or amyloid transthyretin protein) is rare and exhibits an autosomal dominant pattern of inheritance, and the amyloid deposits are composed of[ajnr.org]

  • Tarsal Tunnel Syndrome

    This anomaly appears to be inherited in autosomal dominant fashion with incomplete gene penetrance.[ncbi.nlm.nih.gov] Posttraumatic fibrosis, ganglion cyst, tenosynovitis, tumor of the nerves or other structures, dilated or tortuous veins can cause significant nerve compression in this anatomic[ncbi.nlm.nih.gov] […] by acute erythema, urticaria, vasculitis, purpura, marked exfoliation (peeling), flaccid bullae formation, subepidermal separation/detachment Marfan's syndrome familial, autosomal-dominant[medical-dictionary.thefreedictionary.com]

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