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3,124 Possible Causes for Anemia, Developmental Delay

  • Influenza

    delay, muscular dystrophy, or spinal cord injury].[] Abstract Hemolytic uremic syndrome (HUS) is a disease characterized by thrombotic microangiopathy with a triad of non-immune hemolytic anemia, thrombocytopenia, and renal[] ., anemia, sickle cell anemia) neurologic and neurodevelopmental disorders that affect their ability to swallow and breathe morbid obesity (BMI of 40 or higher) residents[]

  • Wolman Disease

    Common symptoms in infants include enlarged liver and spleen, poor weight gain, low muscle tone, jaundice, vomiting, diarrhea, developmental delay, anemia, and poor absorption[] […] responsible of Wolman disease (WD), a severe systemic disease manifesting in the first days of life with vomiting, diarrhea, failure to thrive, hepatosplenomegaly, jaundice, anemia[] Soon after, they develop signs and symptoms of the disease, which may include: Vomiting Diarrhea Poor weight gain Low muscle tone Developmental delay Enlarged liver and spleen[]

  • Autosomal Recessive Osteopetrosis 7

    Previously existing developmental delays and visual impairment, however, could not be reversed.[] Recessive osteopetrosis commonly manifests in early infancy with macrocephaly, feeding difficulties, evolving blindness and deafness, bone marrow failure, severe anemia, and[] Congenital Dyserythropoietic Anemia.[]

  • Rickets

    delay and ocular dermoids.[] As a result of the official statistics and our research it turned out that children in this age-group more often suffer from intestinal infections, anemia, hypertrophy, rickets[] Hematologic disorders are often observed in common rickets, including hypochromic anemia and the rare Von Jacksch–Luzet syndrome.[]

  • Hypophosphatasia

    Relatively few conditions are associated with a low serum alkaline phosphatase including Wilson's disease, hypophosphatasia, pernicious anemia and untreated hypothyroidism[] delay, and seizures.[] Three clinical types are recognized: [1] infantile (symptoms beginning between birth and 6 months and characterized by severe softening of bones, fever, anemia, vomiting,[]

  • LIG4 Syndrome

    The clinical phenotype shows overlap with a number of other rare syndromes, including Seckel syndrome, Nijmegen breakage syndrome, and Fanconi disease (Fanconi anemia).[] Although four of the five identified patients display immunodeficiency and developmental delay, one patient was developmentally normal.[] anemia: a joint Seattle and Paris analysis of results in 700 patients.[]

  • Hereditary Orotic Aciduria

    In affected patients, main clinical symptoms are a markedly increased urinary excretion of orotic acid combined with megaloblastic anemia.[] delays.[] The ratio of 15.85 differed appreciably from that of 6 patients reported with no megaloblastic anemia.[]

  • Connective Tissue Disease

    delay, seizures Treatment: No effective treatment Hyper- β -aminoisobutyric aciduria (210100) D(R)-3-Aminoisobutyrate:pyruvate aminotransferase Not determined Biochemical[] […] common connective tissue diseases have been listed below: Symptoms of rheumatoid arthritis include painful breathing, shortness of breath, weakness, fatigue, chronic cough, anemia[] delay Treatment: Pyridoxine GABA-transaminase deficiency (137150) 4-Aminobutyrate- α -ketoglutarate aminotransferase ABAT (16p13.3)* Biochemical profile: Elevated plasma[]

  • Hereditary Orotic Aciduria without Megaloblastic Anemia

    Developmental delays may also be noted and may present as growth failure, mental retardation, or motor disorders such as ocular motor dyspraxia.[] Hereditary orotic aciduria without megaloblastic anemia (OAWA) is a very rare genetic disorder. Only four cases have been described to date.[] delays.[]

  • Homocystinuria without Methylmalonic Aciduria Type cblG

    […] cells, or to show macrocytosis without anemia.[] Entire body system Developmental Delay Patients also present diffuse encephalopathy and developmental delays . HMAG patients appear normal at birth.[] Individuals suffering from methionine synthase deficiency have megaloblastic anemia, which is why the disease is also referred to as homocystinuria with megaloblastic anemia[]

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