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11 Possible Causes for Hyperreninemia, Hypothyroidism, Sclerodactyly

  • Systemic Scleroderma

    Visceral organ involvement in lcSSc tends to show insidious progression, and pulmonary arterial hypertension (PAH), interstitial lung disease, hypothyroidism, and primary[accessmedicine.mhmedical.com] SRC is characterized by malignant hypertension, hyperreninemia, azotemia, and microangiopathic hemolytic anemia.[ncbi.nlm.nih.gov] ., 1) sclerodactyly, 2) digital pitting scars of fingertips or loss of substance of the distal finger pad, and 3) bilateral basilar pulmonary fibrosis.[ncbi.nlm.nih.gov]

  • Diffuse Scleroderma

    Hypothyroidism may be associated. Pregnancy [ 22, 23 ] Successful pregnancy is possible. It should be planned when the disease is stable to avoid complications.[patient.co.uk] Symptoms of scleroderma renal crisis are malignant hypertension (high blood pressure with evidence of acute organ damage), hyperreninemia (high renin levels), azotemia (kidney[en.wikipedia.org] , and telangiectasia (CREST) syndrome (disorder) Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) Crest syndrome[icd9data.com]

  • Scleroderma with Renal Involvement

    Hyperreninemia plays a major role in the pathogenesis of SRC.[em-consulte.com] Hypothyroidism Diet Recipes Indicators You Should Try a Gluten Free Diet.png - Get the Entire Hypothyroidism Revolution System Today I definitely have felt grief over this[pinterest.fr] There were no identifiable cutaneous manifestations of scleroderma like sclerodactyly or telangiectasia.[omicsonline.org]

  • Woodhouse Sakati Syndrome

    On the other hand, sustained hypokalemia and hyperreninemia can cause progressive tubulointerstitial nephritis , resulting in end-stage kidney disease (kidney failure).[maria-online.com] PMID 6876115. v t e Endocrine pathology : endocrine diseases ( E00-35, 240-259 ) Thyroid Hypothyroidism ( Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre,[wikidoc.org] Infantile-onset ascending hereditary spastic paralysis Spondyloepimetaphyseal dysplasia x-linked with mental deterioration Limb-girdle muscular dystrophy Palmoplantar keratoderma-sclerodactyly[checkrare.com]

  • Amelo-Onycho-Hypohidrotic Syndrome

    This should also identify hypothyroidism. A positive ANA test with a speckled pattern will help identify scleroderma, but a skin biopsy should also be done.[checkorphan.org] None DOI: 10.4103/ijn.IJN_203_16 Bartter's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia[indianjnephrol.org] […] schisis, schistosomiasis, schizencephaly, schizophrenia, schlegelberger, schmid, schneckenbecken, schofer, schutz, schwannoma, scimitar, sclerae, scleroatonic, sclerocornea, sclerodactyly[rapsodyonline.eurordis.org]

  • Hyperdibasic Aminoaciduria Type 1

    (E03) Other hypothyroidism (E030) Congenital hypothyroidism with diffuse goitre (E031) Congenital hypothyroidism without goitre (E032) Hypothyroidism due to medicaments and[statemaster.com] Galactorrhoea-Hyperprolactinaemia Hyperprolinaemia type 1 Hyperprolinaemia type 2 Hyperprostaglandin E syndrome see Bartter's syndrome Hyperprothrombinemia 20210G-A Hyperreflexia Hyperreninemia[diseaselist.blogspot.com] Infantile-onset ascending hereditary spastic paralysis Spondyloepimetaphyseal dysplasia x-linked with mental deterioration Limb-girdle muscular dystrophy Palmoplantar keratoderma-sclerodactyly[checkrare.com]

  • Periodic Sialadenosis

    […] condition Subseptus uterus Q51.2 Subsiding appendicitis K36 Substernal thyroid E04.9 Substitution disorder F44.9 Subtentorial - see condition Subthyroidism (acquired) - see also Hypothyroidism[icd.codes] Background Bartter syndrome (BS) is a group of inherited, salt-losing tubulopathies presenting as metabolic alkalosis with normotensive hyperreninemia and hyperaldosteronism[researchgate.net] Goiter) 240.9 congenital 759.2 Substitution disorder 300.11 Subtentorial - see condition Subtertian fever 084.0 malaria (fever) 084.0 Subthyroidism (acquired) (see also Hypothyroidism[theodora.com]

  • HIV Wasting Syndrome

    Increased prevalence of subclinical and clinical hypothyroidism in persons with chronic kidney disease. Kidney Int 2005;67:1047-52.[revistanefrologia.com] The proximal site of salt transport defect has been suggested by the absence of hyperreninemia and hypokalemia, which would be a distinguishing feature of Bartter’s syndrome[karger.com] For example, linear scleroderma involving the arm but not crossing any joints is not as functionally limiting as sclerodactyly (scleroderma localized to the fingers).[ssa.gov]

  • Indian Childhood Cirrhosis

    - increased (as well as sodium retention in kidneys) secondary to fall in systemic vascular resistance [13] FibroTest is a biomarker for fibrosis that can be done instead[en.wikipedia.org] Clinical manifestations may include Fanconi syndrome with amino-aciduria, nephrolithiasis, cardiac dysrhythmias, arthritis or arthralgias, rhabdomyolisis, hemolytic anemia, hypothyroidism[medscape.com] グルコース-6-ホスファターゼ欠損症 glucose-6-phosphatase deficiency グルタミン酸尿症(II型) glutamic aciduria (type II) クルベイエル・バウムガルテン症候群 Cruveilhier-Baumgarten syndrome CREST症候群 CREST syndrome 手指硬化 sclerodactyly[jsge.or.jp]

  • Amelogenesis Imperfecta Type 1G with Nephrocalcinosis

    […] syndrome 4 multiple mitochondrial dysfunctions syndrome 5 myofibrillar myopathy 1 myofibrillar myopathy 7 myofibrillar myopathy 8 neonatal diabetes mellitus with congenital hypothyroidism[rgd.mcw.edu] Abstract Bartter's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia with normal[ncbi.nlm.nih.gov] Infantile-onset ascending hereditary spastic paralysis Spondyloepimetaphyseal dysplasia x-linked with mental deterioration Limb-girdle muscular dystrophy Palmoplantar keratoderma-sclerodactyly[checkrare.com]

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