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845 Possible Causes for Anemia, Congenital Alopecia

  • Congenital Syphilis

    In this article, we describe the first occurrence of alopecia in a neonate with congenital syphilis.[ncbi.nlm.nih.gov] Anemia and thrombocytopenia are common hematological findings.[ncbi.nlm.nih.gov] Although rare, bow legs, recurrent fever, anemia, and inflammatory arthralgias may be manifestations of late CS.[ncbi.nlm.nih.gov]

  • Hypothyroidism

    […] of the puppy coat, hyperpigmentation of the skin, and bilaterally symmetric alopecia of the trunk.[web.archive.org] MATERIALS AND METHODS: Patients with toxic nodular goiter and heart failure with concomitant anemia were included.[ncbi.nlm.nih.gov] […] present, usually normocytic-normochromic and of unknown etiology, but it may be hypochromic because of menorrhagia and sometimes macrocytic because of associated pernicious anemia[smartypance.com]

  • Celiac Disease

    anemia.[ncbi.nlm.nih.gov] Congenital heart defects Primary biliary cirrhosis IgA deficiency Isolated hypertransaminasemia Recurrent aphthous stomatitis Myasthenia gravis Recurrent pericarditis Psoriasis[doi.org] Celiac disease may present with hematological abnormalities including long-standing anemia.[ncbi.nlm.nih.gov]

  • Dyskeratosis Congenita

    The case reported is the first in a Negro and showed the previously unrecorded abnormalities: schizophrenia, scarring alopecia, and congenital malformation of the middle ear[jamanetwork.com] At King Faisal Specialist Hospital and Research Center, the most common entity referred for allogeneic hematopoietic cell transplantation (HCT) is Fanconi anemia, followed[ncbi.nlm.nih.gov] Aplastic anemia Aplastic anemia results in progressive bone marrow failure due to the loss of mature blood cells.[cygenia.com]

  • Erythropoietic Porphyria

    Congenital Erythropoietic Porphyria, Erythropoietic Uroporphyria, Porphyria Erythropoietica Congenita, Gunther's Disease, Haematoporphyria Congenita[dermis.net] anemia in a Kashmiri boy.[e-ijd.org] Hair loss 0001596 Autosomal recessive inheritance 0000007 Cholelithiasis Gallstones 0001081 Congenital onset Symptoms present at birth 0003577 Conjunctivitis Pink eye 0000509[rarediseases.info.nih.gov]

  • Multicentric Castleman's Disease

    Case 1: A 57-year-old woman had fever, anemia, anasarca, and some small cervical lymphadenopathy.[ncbi.nlm.nih.gov] […] abnormalities Scleroderma Craniosynostosis alopecia glaucoma and absent frontal sinuses adult SCLC brain defect Hereditary microcornea Sacral hemangiomas Scleromyxedema Craniosynostosis[yumpu.com] Our results indicate that IL-6-induced hepcidin over-production may be involved in the pathophysiology of microcytic anemia commonly observed in this disease.[ncbi.nlm.nih.gov]

  • Hepatoerythropoietic Porphyria

    […] hypoplastic anemia Alopecia Carcinoma Hepatic steatosis Sudden cardiac death Hyperpigmentation of the skin Hypopigmented skin patches Cerebral palsy Fragile skin Scleroderma[mendelian.co] 68-year-old white man (Karnofsky score, 20) 2 with a 36-year history of porphyria and anemia was admitted for severe heart failure (left ventricular ejection fraction, 30[nejm.org] Anemia was present in more than 50% of patients with HEP for whom hematologic status was reported (15 of 27), 2, 6 - 16, 19 - 22, 26, 28, 30, 32, 33 but severe anemia requiring[dx.doi.org]

  • Alopecia

    Congenital triangular alopecia Congenital triangular alopecia references Congenital triangular alopecia Congenital triangular alopecia is a patch of hair loss in the temple[keratin.com] Medical conditions that can cause alopecia Various medical conditions can cause alopecia including: Anemia (low red blood cell count) Anorexia Infections or illnesses Ringworm[web.archive.org] Passed from parents’ genes and the most common cause of hair loss or thinning Hormonal changes: From pregnancy, childbirth or menopause Medical conditions: Thyroid disease, anemia[rush.edu]

  • LIG4 Syndrome

    alopecia, and nail dystrophy T-cell immunodeficiency, congenital alopecia, and nail dystrophy FOXP3base X-linked immunodeficiency, polyendocrinopathy, enteropathy(IPEX) X-linked[hiroshi.mizushima.info] The clinical phenotype shows overlap with a number of other rare syndromes, including Seckel syndrome, Nijmegen breakage syndrome, and Fanconi disease (Fanconi anemia).[humpath.com] anemia: a joint Seattle and Paris analysis of results in 700 patients.[springermedizin.de]

  • Pulmonary Histiocytosis X

    - ECTROPION - RITARDO MENTALE RNG151 SINDROMI CON DISPLASIA ECTODERMICA ITTIOSI A COSTUME DA BAGNO RNG070 ITTIOSI CONGENITE ITTIOSI A ISTRICE GRAVIOR RNG070 ITTIOSI CONGENITE[malattierare.regione.veneto.it] Key terms Anemia — Abnormally low level of red blood cells in the blood. Biopsy — Surgical removal of tissue for examination.[medical-dictionary.thefreedictionary.com] […] clinical feature (nearly 80% of patient will have this) Infiltration of bone marrow and other organs lead to concurrent hepatosplenomegaly, lymphadenopathy, pulmonary lesions, anemia[learningradiology.com]

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