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163 Possible Causes for Autosomal Recessive, Lactate Dehydrogenase Increased, Microcytic Anemia

  • Hereditary Spherocytosis

    Reticulocytosis, increased bilirubin, increased lactate dehydrogenase, increased urinary and fecal urobilinogen, and decreased haptoglobin, reflect increased erythrocyte production[] […] spherocytosis on repeated blood films, Coombs-negative hemolytic jaundice and normal MCHC and MCV measurements, where SDS-PAGE revealed alpha-spectrin deficiency, a rare autosomal-recessive[] anemia of varying degree. [3] Uraninite is a radioactive, uranium-rich mineral and ore with a chemical composition that is largely UO2, but also contains UO3 and oxides of[]

  • Thalassemia

    At the end of the treatment period, Hb and HbF increased by 2.5   1.8 g/dL and 2.5   1.6 g/dL, while bilirubin, lactate dehydrogenase, and the nucleated red blood cell count[] Abstract β-Thalassemia (β-thal) is the most widespread autosomal recessive disorder worldwide.[] Note : Thalassemia is a microcytic, hypochromic anemia. Its cause is a genetically based decreased synthesis of one or several globin chains.[]

  • Cooley's Anemia

    […] and a decreasing trend in the serum lactate dehydrogenase (LDH) and serum unconjugated bilirubin levels.[] recessive trait requiring that both parents pass on a copy of the defective gene located on the chromosome numbered 11.[] The defective gene in Cooley's anemia is on chromosome 11. The insufficient production of the globin chains results in microcytic anemia.[]

  • Iron Deficiency Anemia

    Iron-refractory iron deficiency anemia (IRIDA) is a rare hereditary form of IDA with autosomal recessive inheritance.[] Abstract Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive disease characterized by congenital hypochromic microcytic anemia, low transferrin saturation[] Abstract Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal-recessive disorder hallmarked by hypochromic microcytic anemia, low transferrin saturation, and[]

  • Cecal Adenocarcinoma

    Bloom syndrome is a rare autosomal recessive disorder characterized by short stature, brachydactyly, malar hypoplasia and facial telangiectasia, erythema and cafe au lait[] anemia or has a change in bowel habits, do colonoscopy Metastatic workup: CXR, abdominal CT/ultrasound Bone scan, CT head only if lesions suspected Labs: CBC, urinalysis[] Bloom syndrome is a rare autosomal recessive disorder characterised by short stature, brachydactyly, malar hypoplasia and facial telangiectasia, erythema and cafe au lait[]

  • Adenocarcinoma of the Colon

    Isolated coloboma can also be inherited in an autosomal recessive pattern, which means both copies of a gene in each cell have mutations.[] anemia iron deficiency anemia in an elderly male is colon cancer until proven otherwise fecal occult blood test lacks sensitivity and specificity as it only tests for globin[] Autosomal dominant and autosomal recessive inheritance are found equally in 27 coloboma phenotypes which are not yet mapped, whereas three are supposed to be X-linked.[]

  • Gastric Adenocarcinoma

    […] phosphatase, lactate dehydrogenase, transaminase, and bilirubin ).[] Family segregation analysis with De novo and Autosomal Recessive inheritance model was used to further reduce the number of potential causative variants.[] Mouth sores Diarrhea (may be severe) Less common (10–29% of patients) [ edit ] Poor appetite Nausea and vomiting Hair loss Elevated liver enzymes (temporary increase in alkaline[]

  • Paroxysmal Nocturnal Hemoglobinuria

    The effect of eculizumab on intravascular hemolysis was demonstrated by a reduction in lactate dehydrogenase levels at all measurements after baseline.[] recessive inheritance with incomplete penetrance.22 In a family having 1 sibling with a PDA, there is an 3% chance of a PDA in a subsequent offspring.21 The precise mechanisms[] […] in lactate dehydrogenase levels.[]

  • Lead Poisoning

    We believe that this constellation of clinical and radiographic abnormalities closely resembles osteosclerotic metaphyseal dysplasia (OMD) due to an autosomal recessive defect[] Anemia Leukocytosis Urine microscopy of sediment or renal biopsy Acid-fast inclusion bodies in tubular nuclei Pathognomonic for lead poisoning Free Erythrocyte Protoporphyrin[] Creates a microcytic anemia, with basophilic stippling Often seen concurrently with iron deficiency (GI transporters will more avidly uptake heavy metals in this situation[]

  • Microcytic Anemia

    Most information can be retrieved after the transfusion but it is very helpful to obtain a direct Coombs, iron study, B12 study, lactate dehydrogenase (LDH) and a peripheral[] The objective of the study was to report a novel autosomal recessive lipodystrophy syndrome.[] Causes[edit] Typical causes of microcytic anemia include: Childhood Iron deficiency anemia,[1] by far the most common cause of anemia in general and of microcytic anemia in[]

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