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1,183 Possible Causes for Autosomal Dominant, Iron Deficiency Anemia, Pediatric Disorder

  • Familial Adenomatous Polyposis

    Older paternal age and fresh gene mutation: data on additional disorders. J Pediatr. 1975 Jan. 86(1):84-8. [Medline]. Bisgaard ML, Fenger K, Bülow S, Niebuhr E, Mohr J.[emedicine.medscape.com] English familial adenomatous polyposis autosomal dominant disease that is has material basis in mutations in the APC gene and involves formation of numerous polyps in the[wikidata.org] A 38-year-old lady presented with abdominal pain, diarrhoea and iron deficiency anemia. There was no history of colorectal cancer in the family.[ncbi.nlm.nih.gov]

  • 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[floatinghospital.org] "Blue rubber bleb nevus syndrome" is an autosomal dominant trait characterized by multiple cutaneous and extracutaneous angiomas of dark blue color and rubbery consistency[ncbi.nlm.nih.gov] A 15-year-old girl presented with refractory iron-deficiency anemia (IDA) for 10 years, without any hemorrhagic signs or noticeable cutaneous lesions, which led to her obvious[ncbi.nlm.nih.gov]

  • Hereditary Hemorrhagic Telangiectasia

    The monoclonal antibody bevacizumab, seems to be a good option in this disorder.[ncbi.nlm.nih.gov] BACKGROUND AND OBJECTIVE: Pulmonary arterial hypertension (PAH) is a rare disease that could be inherited with an autosomal dominant pattern.[ncbi.nlm.nih.gov] Bevacizumab, a VEGF inhibitor, reduces epistaxis, telangiectasias, and iron-deficiency anemia.[ncbi.nlm.nih.gov]

  • Gardner Syndrome

    Affiliation: Discipline of Pediatric Otorhinolaryngology, Department of Otorhinolaryngology and Human Communication Disorders, EPM – UNIFESP[scielo.br] Gardner syndrome, a variant of familial adenomatous polyposis, is an autosomal dominant genetic disease characterized by the combined presence of multiple intestinal polyps[ncbi.nlm.nih.gov] Pediatr Int 2003;45:472-4. [ PUBMED ] 5. Campbell AN, Freedman MH, McClure PD. Autoerythrocyte sensitization. J Pediatr 1983;103:157-60. [ PUBMED ] 6.[ijpm.info]

  • 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.[mayomedicallaboratories.com] 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[symptoma.com] Genetic counseling Acute hepatic porphyrias are monogenic hereditary disorders that are transmitted in an autosomal dominant manner (except the hereditary deficit of delta-aminolevulinic[orpha.net]

  • Von Willebrand Disease

    John Akabutu Comprehensice Centre for Bleeding DisordersPediatric Division Stollery Children’s Hospital Clinic Director Dr.[hemophilia.ca] Type 2B von Willebrand disease is also an autosomal dominant trait.[emedicine.medscape.com] Versiti's specialized focus in hematology includes research and diagnostic services for medical conditions such as: anemia, including iron-deficiency anemia; platelet and[bcw.edu]

  • 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[touchoncology.com] In the autosomal dominant form of HS, red cell spectrin levels range from 60-80% of normal.[emedicine.com] METHODS: EMA binding test using flow cytometry was performed on 55 HS (40 families), 26 iron deficiency anemia (IDA), 32 β-thalassemia trait (βTT), and 10 autoimmune hemolytic[ncbi.nlm.nih.gov]

  • 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.[childrenshospital.org] ORPHA:1047 Synonym(s): - Prevalence: Unknown Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive or X-linked dominant or Mitochondrial inheritance[orpha.net] The erythrocytes are hypochromic and microcytic and the iron binding capacity is increased. 280 Iron deficiency anemias 280.0 Iron deficiency anemia secondary to blood loss[icd9data.com]

  • Iron Deficiency Anemia

    Blood Disorders Center, an integrated pediatric hematology and oncology partnership between Dana-Farber Cancer Institute and Boston Children's Hospital.[childrenshospital.org] The latter is an autosomal dominant disorder characterized by distinctive cataracts and HF in the absence of iron overload.[ncbi.nlm.nih.gov] Iron deficiency anemia is a common type of anemia, affecting millions of people worldwide. Iron deficiency anemia is often asymptomatic.[symptoma.com]

  • Food Allergy

    BACKGROUND/AIMS: We evaluated our 16-year single-center experience of pediatric post-transplant lymphoproliferative disorder (PTLD) cases who underwent liver transplantation[ncbi.nlm.nih.gov] People with autosomal dominant hyper-immunoglobulin E syndrome (HIES) have recurrent bacterial infections of the skin and lungs.[niaid.nih.gov] The prevalence of nonclassic celiac disease is high in the Western world, with patients mainly presenting with unexplained iron-deficiency anemia.[web.archive.org]

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