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1,064 Possible Causes for Autosomal Dominant, Iron Increased, Pediatric Disorder

  • Hereditary Spherocytosis

    The 2003 Healthcare Cost and Utilization Project (HCUP) Kids’ Inpatient Database (KID), a robust and widely used measure of pediatric disorders, has estimated that the number[] In the autosomal dominant form of HS, red cell spectrin levels range from 60-80% of normal.[] Indications for laparoscopic removal of the spleen included anemia unresponsive to iron supplementation in eight patients (66.6 %) with increase need for red cells transfusions[]

  • Acute Hepatic Porphyria

    Tortorelli S, Kloke K, Raymond K: Chapter 15: Disorders of porphyrin metabolism. In Biochemical and Molecular Basis of Pediatric Disease. Fourth edition.[] Apart from an autosomal recessive pattern of inheritance seen in ADP, all hepatic porphyrias are caused by autosomal dominant mutations, leading to accumulation of neurotoxic[] […] hepatic iron store s, hemochromatosis Alcoho l, smoking Hepatitis C HIV Estrogen therapy Sunlight exposure Pathophysiology Clinical findings Cutaneous manifestations Increased[]

  • Erythropoietic Coproporphyria

    Tortorelli S, Kloke K, Raymond K: Chapter 15: Disorders of porphyrin metabolism. In Biochemical and Molecular Basis of Pediatric Disease. Fourth edition.[] dominant ) Hereditary coproporphyria ( autosomal dominant ) Doss porphyria ( autosomal recessive ) Chronic hepatic porphyrias Porphyria cutanea tarda ; ( autosomal dominant[] "Disorders of Porphyrin Metabolism". In Dietzen, Dennis J; Bennett, Michael J.; Wong, Edward C. (eds.). Biochemical and Molecular Basis of Pediatric Disease (4th ed.).[]

  • Iron Deficiency Anemia

    Blood Disorders Center, an integrated pediatric hematology and oncology partnership between Dana-Farber Cancer Institute and Boston Children's Hospital.[] The latter is an autosomal dominant disorder characterized by distinctive cataracts and HF in the absence of iron overload.[] This is because your need for iron increases during these times of growth and development.[]

  • Acute Myelocytic Leukemia

    Hasle H: Myelodysplastic and myeloproliferative disorders in children. Curr Opin Pediatr 19 (1): 1-8, 2007.[] dominant mode of genetic transmission.[] An iron stain usually shows increased iron stores and may show ring sideroblasts (Figure 2, B [inset]).[]

  • Anemia

    One of the most common pediatric disorders, anemia has many potential causes. Anemia is often a symptom of a disease rather than a disease itself.[] ORPHA:1047 Synonym(s): - Prevalence: Unknown Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive or X-linked dominant or Mitochondrial inheritance[] Often athletes who are concerned about being iron deficient or think that increased iron levels can increase performance will jump immediately to iron supplements.[]

  • Cystic Fibrosis

    Children's is home to the leading pediatric pulmonology program in Georgia.[] Besides, there was a rare association with autosomal dominant type of polycystic renal disease.[] The current management of this condition includes the use of regular red blood cell transfusions and iron chelation therapy.[]

  • Leukemia

    […] oncologist at Dana-Farber/Boston Children’s Cancer and Blood Disorders Center.[] dominant human disorder with multiple café-au-lait spots, axillary freckling, macrocephaly, and learning difficulties. 1, 2 This disorder belongs to the recently identified[] Leukemia is the most common form of pediatric cancer. It affects approximately 3,250 children each year in the US, accounting for about 30 percent of childhood cancers.[]

  • Blue Rubber Bleb Nevus Syndrome

    Phone: 617-636-5025 Fax #: 617-636-8122 Pediatric surgery, pediatric trauma, congenital disorders requiring surgery in newborns, GI inflammatory diseases in children, pediatric[] "Blue rubber bleb nevus syndrome" is an autosomal dominant trait characterized by multiple cutaneous and extracutaneous angiomas of dark blue color and rubbery consistency[] After supplementation with intravenous iron for 1 month without other interventions, hemoglobin levels had increased to 87 g/L.[]

  • Glycogen Storage Disease Type 1

    Nelson Textbook of Pediatrics. 16th ed. Philadelphia: Saunders; 2000. p. 405. 6. Bickel H, Manz F.[] Amyloidosis with renal failure is a complication and may develop without overt crises ( French FMF Consortium, 1997 ).See also autosomal dominant FMF ( OMIM ), which is caused[] […] patients with inheritable metabolic disorders.[]

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