Create issue ticket

62 Possible Causes for Bicytopenia, Failure to Thrive

  • Gaucher Disease

    The various symptoms and the age when they are most likely to present are as follows: [4] Newborn Congenital ichthyosis Organomegaly Failure to thrive Brain stem dysfunction[] Failure to thrive and stridor (due to laryngospasm) are also common.[] Failure to thrive, swallowing abnormalities, oculomotor apraxia, hepatosplenomegaly, and stridor due to laryngospasm are typical in infants with type 2 disease.[]

  • Vitamin B12 Deficiency

    Laboratory data revealed bicytopenia with macrocytic anemia and methylmalonic acid in the urine, consistent with vitamin B12 deficient anemia.[] When preventive supplementation has failed, one should recognize and treat quickly an infant presenting with failure to thrive and delayed development.[] Vitamin B12 deficiency is rare in children, with nonspecific symptoms including failure to thrive, vomiting, anorexia, and neurologic changes with or without hematologic disturbances[]

  • Pancytopenia

    […] of bicytopenia and pancytopenia.[] Blood 2015 125:1840; doi: A 4-year-old girl with a known history of methylmalonic acidemia (MMA) complicated by acquired hypothyroidism, failure to thrive, and developmental[] If more than one of the blood cells is low then the condition is called as bicytopenia.[]

  • Lymphopenic Agammaglobulinemia - Short-Limbed Dwarfism Syndrome

    Copper deficiency can cause neutropenia in patients on total parenteral nutrition, with a history of gastrectomy, and in malnourished children 86, 87, 88 and the bicytopenia[] […] to thrive).[] Additional clues to immunodeficiency include: failure to thrive with or without chronic diarrhea, persistent infections after receiving live vaccines, and chronic oral or[]

  • Adenosine Deaminase Deficiency

    Because patient 5 had bicytopenia during admission, a bone marrow aspiration was performed and the diagnosis was myelofibrosis.[] A first-born baby boy presented at age 3 months with persistent diarrhoea, failure to thrive, and recurrent bacterial and fungal infections.[] Infants exhibit failure to thrive, growth failure, chronic diarrhea, and absence of tonsils and lymph nodes.[]

  • Hypocupremia

    Bone marrow aspirate done to evaluate the cause of bicytopenia revealed trilineage dysplasia.[] Signs and symptoms : Signs and symptoms include failure to thrive, pallor, anemia, muscular hypotonia, short stature, repeated seizures, acne, deep philtrum, wide nasal bridge[] Copper deficiency usually presents with bicytopenia (neutropenia and anemia), but severe pancytopenia has been observed in some cases, especially those patients on TPN.[]

  • Chronic Myeloid Leukemia

    In contrast to patients with RA and only dyserythropoiesis, patients with multilineage dysplasia have bicytopenia or pancytopenia, a higher incidence of cytogenetic abnormalities[]

  • Idiopathic Refractory Anemia

    My Response Distinguishing Cases of Immune-Mediated BM failure Diagnosing MDS is often challenging in patients with pancytopenia or bicytopenia who do not show definitive[] Fred Ferri’s popular "5 books in 1" format provides quick guidance on menorrhagia, Failure to Thrive (FTT), Cogan’s syndrome, and much more.[] The terms “ICUS-anemia, ICUS-neutropenia, ICUS-thrombocytopenia, ICUS-bicytopenia, or bi/pancytopenia” were also proposed in which the cut-off levels of cytopenia were the[]

  • Sepsis

    DIAGNOSIS: The present patient met 5 of the HLH criteria: fever, splenomegaly, bicytopenia, hypertriglyceridemia and/or hypofibrinogenemia, and hyperferritinemia.[] Diagnosis usually follows several infections, or a child's failure to thrive.[] Clinical description SCID usually presents within the first few months of life with failure to thrive, severe infections (pneumonia, gastrointestinal infections, sepsis),[]

  • Familial Neutropenia

    RCUD and MDS-U categories in 196 patients with less than 5% marrow blasts, Maassen et al. found 28% RA, 6% RT, 13% RN, 20% patients with no cytopenia, and 34% patients with bicytopenia[] Fred Ferri’s popular "5 books in 1" format provides quick guidance on menorrhagia, Failure to Thrive (FTT), Cogan’s syndrome, and much more.[] Diagnosis is usually made during the first months of life as SDS babies exhibit a failure to thrive, feeding problems and lowered blood cell counts. [6] Chediak-Higashi Syndrome[]

Further symptoms

Similar symptoms