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26 Possible Causes for Alkaline Phosphatase Increased, Cataracts Usually Congenital

  • Hemochromatosis

    […] levels usually normal or low) II.[faculty.washington.edu] cataracts) Neuroferritinopathy (autosomal dominant genetic disorder affecting basal ganglai; clinical onset in adulthood, iron and ferritin deposits in the brain, ferritin[faculty.washington.edu] H-ferritin mutation Hyperferritinemia without iron overload (autosomal dominant genetic disorder causing high ferritin levels without iron overload; associated with bilateral congenital[faculty.washington.edu]

  • Fanconi Renotubular Syndrome

    Lowe's syndrome A rare inherited disorder that is distinguished by congenital cataracts, glaucoma, and severe mental retardation.[the-medical-dictionary.com] phosphatase Greatly elevated alkaline phosphatase High serum alkaline phosphatase Increased alkaline phosphatase Increased serum alkaline phosphatase Last updated: 2/27/2017[rarediseases.info.nih.gov] […] alterations involving the eyes, central nervous system (CNS), and kidneys.5-7 Certain clinical manifestations are usually present, including congenital cataract and glaucoma[bjn.org.br]

  • Congenital Cataract

    What percentage of congenital cataracts are inherited and part of syndromes? Bilateral congenital cataracts are usually inherited or acquired?[quizlet.com] Creatine kinase and serum alkaline phosphatase may be increased and muscle histology shows small, atrophic fibers with increased fibrosis and considerable variations in fiber[disorders.eyes.arizona.edu] Overview Background A cataract is an opacification of the lens. Congenital cataracts usually are diagnosed at birth.[emedicine.medscape.com]

  • Congenital Liver Cirrhosis

    Congenital hepatic fibrosis (CHF) usually presents with signs and symptoms of portal hypertension, although cases presenting in infancy with cholestasis are well known [8][indianpediatrics.net] A diagnosis of CHF is suggested when normal hepatocellular function is associated with hypersplenism and increased levels of alkaline phosphatase and gamma glutamyl transferase[jmedicalcasereports.biomedcentral.com] […] in twin pregnancies Alkaline phosphatase levels rise three- to fourfold because of placental production Clotting factors I, II, V, VII, VIII, X, and XII Ceruloplasmin level[clevelandclinicmeded.com]

  • Distal Myopathy Type 3

    In some people, the condition can also cause cataracts to develop at a younger age than usual. Life expectancy for people with myotonic dystrophy can vary considerably.[nhs.uk] (400 to 1165) Serum Alkaline phosphatase: High with Paget disease EMG: Variable Myopathy: Small amplitude, Polyphasic Brief motor unit potentials Spontaneous activity: Fibrillations[neuromuscular.wustl.edu] I obtain a baseline complete blood count (CBC) and differential, platelet count, and serum glutamic pyruvic transaminase (SGPT) and alkaline phosphatase levels levels.[sites.google.com]

  • Congenital Neutropenia

    In this form, with dominant transmission related to the mutation in the dynamin 2 gene, neurological signs are sometimes discreet and are accompanied by congenital cataract[ojrd.biomedcentral.com] […] blood alkaline phosphatase, and headache with severe chronic neutropenia are arthralgia, bone pain, back pain, muscle spasms, musculoskeletal pain, pain in extremity, splenomegaly[neupogenhcp.com] Diagnosis of congenital neutropenia Neutropenia is a relatively frequent finding, while congenital neutropenia is quite rare.[ojrd.biomedcentral.com]

  • Renal Tubular Acidosis

    Lowe's syndrome — A rare inherited disorder that is distinguished by congenital cataracts, glaucoma, and severe mental retardation.[medical-dictionary.thefreedictionary.com] Other significant laboratory findings may include decreased sodium bicarbonate, pH, potassium, and phosphorus; increased serum chloride, alkaline phosphatase, urinary bicarbonate[medical-dictionary.thefreedictionary.com] Rickets — A deficiency disease that affects the bone development of growing bodies, usually causing soft bones. acidosis [ as″ĭ-do sis ] 1. the accumulation of acid and hydrogen[medical-dictionary.thefreedictionary.com]

  • Craniosynostosis-Dandy-Walker Malformation-Hydrocephalus Syndrome

    Walker-Warburg Syndrome Clinical Characteristics Ocular Features: The eyes are usually small and contain either retinal dysplasia or a congenital retinal detachment.[disorders.eyes.arizona.edu] P253R and nonsyndromic craniosynostosis osteoblasts showed a marked differentiated phenotype , characterized by high alkaline phosphatase activity, increased mineralization[ihop-net.org] Colobomas, PHPV, cataracts, glaucoma, buphthalmos, anterior chamber dysgenesis, optic atrophy, and optic nerve hypoplasia have also been reported.[disorders.eyes.arizona.edu]

  • Distal Renal Tubular Acidosis

    Lowe's syndrome — A rare inherited disorder that is distinguished by congenital cataracts, glaucoma, and severe mental retardation.[medical-dictionary.thefreedictionary.com] Other significant laboratory findings may include decreased sodium bicarbonate, pH, potassium, and phosphorus; increased serum chloride, alkaline phosphatase, urinary bicarbonate[medical-dictionary.thefreedictionary.com] Rickets — A deficiency disease that affects the bone development of growing bodies, usually causing soft bones. acidosis [ as″ĭ-do sis ] 1. the accumulation of acid and hydrogen[medical-dictionary.thefreedictionary.com]

  • Alagille Syndrome

    , congenital deafness, neurosensory nephropathy Comment Alport syndrome is characterized by haematuric nephropathy, in most cases leading to renal failure (usually progressive[doi.org] Increased serum concentrations of bile acids, alkaline phosphatase, gamma-glutamyl transpeptidase (GGT), triglycerides, and the aminotransferases are also seen.[ncbi.nlm.nih.gov] […] oesophageal leiomyoma gastric leiomyoma leiomyoma of the clitoris leiomyoma of the urethra trachea, leiomyoma of the uterine leiomyoma vulvar leiomyoma Non-tumour features: cataract[doi.org]

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