Endocrine, Nutritional and Metabolic Disease Introduction: Idiopathic Hypoglycemia, Biotin Deficiency, Pseudopseudohypoparathyroidism Source Wikipedia

ISBN: 9781156976272

Published: August 30th 2011

Paperback

28 pages


Description

Endocrine, Nutritional and Metabolic Disease Introduction: Idiopathic Hypoglycemia, Biotin Deficiency, Pseudopseudohypoparathyroidism  by  Source Wikipedia

Endocrine, Nutritional and Metabolic Disease Introduction: Idiopathic Hypoglycemia, Biotin Deficiency, Pseudopseudohypoparathyroidism by Source Wikipedia
August 30th 2011 | Paperback | PDF, EPUB, FB2, DjVu, talking book, mp3, ZIP | 28 pages | ISBN: 9781156976272 | 8.38 Mb

Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 26. Chapters: Idiopathic hypoglycemia, Biotin deficiency, Pseudopseudohypoparathyroidism, Albrights hereditaryMorePlease note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 26. Chapters: Idiopathic hypoglycemia, Biotin deficiency, Pseudopseudohypoparathyroidism, Albrights hereditary osteodystrophy, Conns Syndrome, Sheehans syndrome, Ochronosis, Hyperinsulinemia, Impaired fasting glucose, Pyruvate dehydrogenase deficiency, Fatty-acid metabolism disorder, Permanent neonatal diabetes mellitus, Sphincter of Oddi dysfunction, Glycogen storage disease type VI, De Quervains thyroiditis, MODY 5, Adiposogenital dystrophy, Glucocorticoid deficiency 1, MODY 2, Finnish type amyloidosis, Pituitary disease, Testicular disease, MODY 1, Glycogen storage disease type IV, Toxic multinodular goiter, Essential fructosuria, Glycoproteinosis, Adrenocorticotropic hormone deficiency, Histidinemia, MODY 3, Glycogen storage disease type XI, Piebaldism, Keshan disease, Thyroid dyshormonogenesis, Postpartum thyroiditis, Hyperpituitarism, Enolase deficiency, Abscess of thymus, Proximal diabetic neuropathy, MODY 6, Glycogen storage disease type IX, Glycogen storage disease type 0, Diabetes mellitus and deafness, Pentosuria, Autoimmune adrenalitis, Aldolase A deficiency, Zamia staggers, Tertiary hyperparathyroidism, Pseudohypoaldosteronism, Pituitary ACTH hypersecretion, Toxic nodular goitre, MODY 4, Acute infectious thyroiditis, Hypophysitis, Methylmalonyl-CoA mutase deficiency, Transaldolase deficiency, Hypoestrogenism, Parathyroiditis, Subacute thyroiditis, Hypothalamic disease, Endocrine bone disease, 6-phosphogluconate dehydrogenase deficiency, Amyloid degeneration, Adrenocortical hyperfunction, Autoimmune thyroiditis, Juvenile diabetes mellitus, Thymic hypoplasia, Endocrine paraneoplastic syndrome.

Excerpt: Biotin deficiency is a rare nutritional disorder which can become serious, even fatal, if allowed to progress untreated. It can occur in people of any age, ancestry, or gender. Biotin deficiency rarely occurs among he...



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