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8,413 Possible Causes for Anemia, Mutation in the Endoglin Gene, Pharyngeal Hemorrhage

  • Hereditary Hemorrhagic Telangiectasia

    In addition, genetic linkage studies and/or mutation analysis identified endoglin as the disease-causing gene in 6 of these families.[pediatrics.aappublications.org] INTRODUCTION: Cardiac phenotypes should be pronounced in hereditary hemorrhagic telangiectasia (HHT) due to frequent systemic arteriovenous malformations (AVMs), iron deficiency anemia[ncbi.nlm.nih.gov] A genetic test, identifying the mutation in endoglin gene both in the patient and in the father, confirmed the suspected diagnosis of HHT.[ncbi.nlm.nih.gov]

  • Upper Gastrointestinal Bleeding

    CONCLUSION: This study did not uncover relationships between anemia and HRQoL or anemia and fatigue after nonvariceal AUGIB.[ncbi.nlm.nih.gov] Severe Alcohol Withdrawal Syndrome Sexual Abuse, Child Shoulder Instability Sinusitis Sleep Apnea Splenomegaly Streptococcal Pharyngitis Stroke Stroke, Hemorrhagic Temporal[jamaevidence.mhmedical.com] Arteriovenous malformations of the stomach are rare; blood loss may be manifested either by chronic anemia or by massive recurrent hemorrhage.[ncbi.nlm.nih.gov]

    Missing: Mutation in the Endoglin Gene
  • Hyperglobulinemic Purpura

    McAllister KA, Baldwin MA, Thukkani AK, et al: Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect[medtextfree.wordpress.com] […] and aplastic anemia.[ijdr.in] […] skin necrosis is characteristic Usually follows some acute infectious disease such as scarlet fever, strep pharyngitis, and meningococcal meningitis, varicella. 46 Purpura[slideplayer.com]

  • Ulcerative Colitis

    This patient was evaluated for iron deficiency anemia and underwent hemicolectomy for extensive right-side predominant inflammatory pseudopolyps.[ncbi.nlm.nih.gov] (n 1) Placebo (N 34): Total with adverse effects 5; vaginitis (n 1), edema (n 1), gastroenteritis (n 1), rectal hemorrhage (n 1), urinary tract infection (n 1), chest pain[doi.org] Complete blood cell count and blood chemistries may be ordered, looking for anemia (low red blood cell count) and other abnormalities, including those from dehydration.[doi.org]

    Missing: Mutation in the Endoglin Gene
  • Infectious Mononucleosis

    An 18-year-old woman with infectious mononucleosis developed splenic infarction and severe anemia.[ncbi.nlm.nih.gov] The hemorrhagic pharyngeal tonsils with hot signals on 18F-fluorodeoxyglucose-positron emission tomography-computed tomography were biopsied revealing the presence of EBV-encoded[ncbi.nlm.nih.gov] Infectious mononucleosis (IM) is a rare cause of aplastic anemia in adults.[ncbi.nlm.nih.gov]

    Missing: Mutation in the Endoglin Gene
  • Throat Cancer

    Adverse events included anemia, neutropenia, infection, nausea, vomiting, anorexia, and fatigue.[web.archive.org] The most common hematologic toxicity (HTOX) was grade 1–2 anemia (26.1%). Nonhematologic toxicities (NHTOX) were mild and manageable.[journals.lww.com] High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia. Arch Otolaryngol Head Neck Surg 2003 ; 129 : 106 –12.[doi.org]

    Missing: Mutation in the Endoglin Gene
  • Temporal Arteritis

    It presents with headache, fever, elevated erythrocyte sedimentation rate and anemia.[ncbi.nlm.nih.gov] Severe Alcohol Withdrawal Syndrome Sexual Abuse, Child Shoulder Instability Sinusitis Sleep Apnea Splenomegaly Streptococcal Pharyngitis Stroke Stroke, Hemorrhagic Temporal[jamaevidence.mhmedical.com] Neurological examination disclosed chin hypoesthesia while investigations showed a normocytic anemia, ESR of 100, and CRP of 72.[ncbi.nlm.nih.gov]

    Missing: Mutation in the Endoglin Gene
  • Congenital Aplastic Anemia

    A seven-year-old girl with Fanconi's anemia-like congenital aplastic anemia and concurrent asplenia without the congenital heart defects or the abdominal heterotaxia is reported[ncbi.nlm.nih.gov] She had hemorrhagic painful blisters on lips and buccal mucosa, pharyngeal erythema with enlarged inflamed tonsils without exudates, and shotty non tender bilateral anterior[omicsonline.org] For instance, CAA may be observed in individuals suffering from Fanconi anemia, Diamond-Blackfan anemia, and Shwachman-Diamond syndrome.[symptoma.com]

    Missing: Mutation in the Endoglin Gene
  • Constitutional Anemia due to Iron Metabolism Disorder

    […] to unexplained anemia.[emedicine.medscape.com] Mutations in two genes, endoglin and ALK-1, have been shown to be responsible for pure HHT, with the disease subtypes designated HHT1 and HHT2.[aetna.com] Your doctor will diagnose anemia with a physical exam and blood tests. Treatment depends on the kind of anemia you have.[medicbind.com]

    Missing: Pharyngeal Hemorrhage
  • Carcinoma of the Larynx

    […] alcohol use poor nutrition human papillomavirus exposure immune system problems workplace exposure to toxins, such as asbestos certain genetic diseases, such as Fanconi anemia[healthline.com] High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia. Arch Otolaryngol Head Neck Surg. 2003;129:106-112.[cancer.org] Anemia decreases the body’s ability to transport oxygen to the body’s organs.[news.cancerconnect.com]

    Missing: Mutation in the Endoglin Gene

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