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Home > Art, Film & Photography > Cell Surface Receptor Deficiencies: Achondroplasia, Cenani Lenz Syndactylism, Hereditary Hemorrhagic Telangiectasia
Cell Surface Receptor Deficiencies: Achondroplasia, Cenani Lenz Syndactylism, Hereditary Hemorrhagic Telangiectasia

Cell Surface Receptor Deficiencies: Achondroplasia, Cenani Lenz Syndactylism, Hereditary Hemorrhagic Telangiectasia


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About the Book

Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 35. Chapters: Achondroplasia, Cenani Lenz syndactylism, Hereditary hemorrhagic telangiectasia, Wolff-Parkinson-White syndrome, Kallmann syndrome, ABCD syndrome, Robinow syndrome, Donnai-Barrow syndrome, Crouzon syndrome, Leber's congenital amaurosis, Achondroplasia in children, Congenital hypothyroidism, Aarskog-Scott syndrome, Apert syndrome, Laron syndrome, X-linked severe combined immunodeficiency, Nevoid basal cell carcinoma syndrome, Persistent Mullerian duct syndrome, Pseudopseudohypoparathyroidism, XX gonadal dysgenesis, Antley-Bixler syndrome, Loeys-Dietz syndrome, Juvenile polyposis syndrome, Thanatophoric dysplasia, Jansen's metaphyseal chondrodysplasia, Congenital amegakaryocytic thrombocytopenia, Jackson-Weiss syndrome, Familial hypocalciuric hypercalcemia, Hypochondroplasia, Pfeiffer syndrome, Muenke syndrome, Male-limited precocious puberty, Hyper-IgM syndrome type 3. Excerpt: Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease and Osler-Weber-Rendu syndrome, is a genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver and brain. It may lead to nosebleeds, acute and chronic digestive tract bleeding, and various problems due to the involvement of other organs. Treatment focuses on reducing bleeding from blood vessel lesions, and sometimes surgery or other targeted interventions to remove arteriovenous malformations in organs. Chronic bleeding often requires iron supplements and sometimes blood transfusions. HHT is transmitted in an autosomal dominant fashion, and occurs in one in 5,000 people. The disease carries the names of Sir William Osler, Henri Jules Louis Marie Rendu and Frederick Parkes Weber, who described it in the late 19th and early 20th centuries. Tongue telangiectases as seen in a person w...


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Product Details
  • ISBN-13: 9781233144334
  • Publisher: Books LLC, Wiki Series
  • Publisher Imprint: Books LLC, Wiki Series
  • Height: 246 mm
  • No of Pages: 36
  • Spine Width: 2 mm
  • Weight: 82 gr
  • ISBN-10: 1233144332
  • Publisher Date: 20 Aug 2011
  • Binding: Paperback
  • Language: English
  • Returnable: N
  • Sub Title: Achondroplasia, Cenani Lenz Syndactylism, Hereditary Hemorrhagic Telangiectasia
  • Width: 189 mm


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