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1,066 Possible Causes for Autosomal Dominant, Leukocytosis, 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[touchoncology.com] In the autosomal dominant form of HS, red cell spectrin levels range from 60-80% of normal.[emedicine.com] Reticulocytosis of 15 to 30% and leukocytosis are common.[merckmanuals.com]

  • Cryopyrin-Associated Periodic Syndrome

    Author information 1 a Division of Pediatric Rheumatology, Reference Center for Autoinflammatory Disorders CEREMAI, Bicêtre Hospital, University of Paris SUD, Le Kremlin Bicêtre[ncbi.nlm.nih.gov] The disease was inherited as an autosomal dominant trait.[ncbi.nlm.nih.gov] Diagnostic methods Diagnosis is based on clinical manifestations and on laboratory findings revealing generalized leukocytosis and neurophilia along with others elevated acute[orpha.net]

  • 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] Because the pain is neuropathic, it often is not accompanied by fever or leukocytosis.[hematologyandoncology.net]

  • Erythropoietic Coproporphyria

    Tortorelli S, Kloke K, Raymond K: Chapter 15: Disorders of porphyrin metabolism. In Biochemical and Molecular Basis of Pediatric Disease. Fourth edition.[mayomedicallaboratories.com] dominant ) Hereditary coproporphyria ( autosomal dominant ) Doss porphyria ( autosomal recessive ) Chronic hepatic porphyrias Porphyria cutanea tarda ; ( autosomal dominant[amboss.com] (iii) Periodic attacks of abdominal pain which is associated with fever and leukocytosis.[biologydiscussion.com]

  • Familial Mediterranean Fever

    […] doi: 10.1097/BOR.0000000000000315 PEDIATRIC AND HERITABLE DISORDERS: Edited by Polly J.[journals.lww.com] […] that mimics autosomal dominant inheritance.[ghr.nlm.nih.gov] During these attacks she had leukopenia and neutropenia instead of leukocytosis.[ncbi.nlm.nih.gov]

  • Acute Myelocytic Leukemia

    Hasle H: Myelodysplastic and myeloproliferative disorders in children. Curr Opin Pediatr 19 (1): 1-8, 2007.[northshore.org] dominant mode of genetic transmission.[ncbi.nlm.nih.gov] Thus, the bone marrow and peripheral blood are characterized by leukocytosis with a predominance of immature cells, primarily blasts.[ncbi.nlm.nih.gov]

  • Leukemia

    […] oncologist at Dana-Farber/Boston Children’s Cancer and Blood Disorders Center.[theguardian.com] dominant human disorder with multiple café-au-lait spots, axillary freckling, macrocephaly, and learning difficulties. 1, 2 This disorder belongs to the recently identified[doi.org] Evaluation Step 0: Leukocytosis ( White Blood Cell Count 11,000/mm3) Confirmed with a second Complete Blood Count with differential No other obvious cause for Leukocytosis[fpnotebook.com]

  • Osteomyelitis

    Pediatr Infect Dis J 15: 725. [Crossref] Deely DM, Schweitzer ME (1997) MR imaging of bone marrow disorders. Radiol Clin North Am 35: 193-212.[oatext.com] […] recessive form is "malignant" with anemia, manifests at birth; autosomal dominant form is "benign" Malignant form is more dramatic, with severe impairment and systemic complications[pathologyoutlines.com] […] indication considered when radiography is unrevealing findigs may reveal bone necrosis, abscess, and sinus tracts Studies Labs C-reactive protein erythrocyte sedimentation rate leukocytosis[step2.medbullets.com]

  • Familial Neutropenia

    […] physician involved in the diagnosis of pediatric bone marrow disorders.[books.google.de] Pedigrees of four of these families were also studied, which pointed to an autosomal dominant form of inheritance.[cags.org.ae] .: Leukaemoid reaction: lymphocytic monocytic myelocytic Leukocytosis Lymphocytosis (symptomatic) Lymphopenia Monocytosis (symptomatic) Plasmacytosis D72.9 Disorder of white[icd.who.int]

  • Splenic Rupture

    Vascular Ehlers-Danlos Syndrome (VEDS) is a rare autosomal dominant collagen vascular disorder.[ncbi.nlm.nih.gov] […] result of irritation of the diaphragm Physical exam hypotension shock Differential Splenic abscess seen in immunocompremised patients and IV drug users presents with fever, leukocytosis[medbullets.com] (see differential diagnoses below) References: [3] Diagnostics Laboratory tests : low Hb, leukocytosis, and thrombocytosis ; crossmatch for blood transfusion if needed In[amboss.com]

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