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         Bassen-kornzweig Syndrome:     more detail
  1. Bassen-Kornzweig syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Bryan, PhD Cobb, 2005

101. Neurology -- Correspondence For Houlden Et Al., 61 (10) 1423-1426
This conflicts with the use of “abetalipoproteinemia” (ABL, Bassen Kornzweig syndrome; MIM 200100) and “homozygous hypobetalipoproteinemia” (FHBL,
http://www.neurology.org/cgi/eletters/61/10/1423
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H. Houlden, S. Lincoln, M. Farrer, P.G. Cleland, J. Hardy, and R.W. Orrell
Compound heterozygous mutations confirm HARP and Hallervorden-Spatz syndromes are allelic
Neurology 2003; 61: 1423-1426 [Abstract] [Full text] [PDF]
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Correspondence published:
Reply to Danek et al
Richard W Orrell, Henry Houlden, Jim S Owen (18 February 2004)
Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic
Adrian Danek, MD, Robert A. Hegele, MD, FRCP, FACP (18 February 2004)
Reply to Danek et al 18 February 2004 Richard W Orrell

102. GASNet Anesthesiology: Contents H - L
Bassen Kornzweig syndrome. Köhlmeier. Köhlmeier - Degos Disease (Malignant Atrophic Papulosis). Krabbe. Krabbe s Disease (Globoid Cell Leukodystrophy)
http://www.gasnet.org/pediatric-syndromes/h2l_br.php
Contents H - L - pediatric syndromes - Hallerman Hallerman - Streiff Syndrome Hallervorden Hallervorden - Spatz Disease Hand Holt - Oram Syndrome (Heart - Hand Syndrome) Hand Hand - Schuller - Christian Disease (Histiocytosis X) Harlequin Ichtyosiform Erythrodermia (Harlequin fetus) Heart Holt - Oram Syndrome (Heart - Hand Syndrome) Hemochromatosis Hemochromatosis Hemolytic Uremic Syndrome Hemolytic Uremic Syndrome Henoch Henoch - Schönlein Purpura Hereditary Hereditary Angioneurotic Edema Hers Hers Disease (Type VI Glycogen Storage Disease) Higashi Chediak - Higashi Syndrome Hippel Von Hippel - Lindau Syndrome Histiocytosis Hand - Schuller - Christian Disease (Histiocytosis X) Histiocytosis Letterer - Siwe Disease (Acute Disseminated Histiocytosis) Hoffman Werdnig - Hoffman Disease Holt Holt - Oram Syndrome (Heart - Hand Syndrome) Holoprosencephaly Holoprosencephaly Homocystinuria Homocystinuria Hunter Hunter's Syndrome (Mucopolysaccharidosis Type II) Hurler Hurler Syndrome (Mucopolysaccharidosis Type I) Hutchinson Progeria (Hutchinson - Gilford Syndrome) Hypothyroidism Cretinism (Congenital Hypothyroidism) Ichtyosiform Ichtyosiform Erythrodermia (Harlequin fetus) Ivemark Ivemark Syndrome Jampel Schwartz - Jampel Syndrome Jervell Jervell and Lange - Nielsen Syndrome Jeune Jeune's Syndrome (Asphyxiating Thoracic Dystrophy) Johnson Erythema Multiforme Major (Stevens - Johnson Syndrome) Kartagener Kartagener's Syndrome (Immotile Cilia Syndrome) Kasabach Kasabach - Merritt Syndrome Kawasaki Kawasaki's Disease Ketonuria Maple Syrup Urine Disease (Branched Chain Ketonuria) King

103. GASNet Anesthesiology: Contents A - C
Bartter syndrome. Bassen. Bassen Kornzweig syndrome. Beckwith. Beckwith - Wiedemann syndrome. Behçet. Behçet syndrome. Blackfan
http://www.gasnet.org/pediatric-syndromes/a2c_br.php
Contents A - C - pediatric syndromes - Acidosis Fanconi's Syndrome (Renal Tubular Acidosis) Albers Albers - Schönberg Disease (Osteopetrosis, Marble Bone Disease) Albright Albright - Butler Syndrome (Primary Distal Renal Tubular Acidosis) Albright McCune - Albright Syndrome Aldrich Wiskott - Aldrich Alström Alström Syndrome Analbumenia Analbumenia Analphalipoproteinemia Tangier Disease (Analphalipoproteinemia) Andersen Andersen Disease (Glycogen Storage Disease Type IV) Anderson Anderson Syndrome Angelman Angelman's Syndrome Angioneurotic Hereditary Angioneurotic Edema Angioosteohypertrophy Klippel - Trenaunay Syndrome (Angioosteohypertrophy) Anhydrotic Christ - Siemens - Touraine Syndrome (Anhydrotic Ectodermal Dysplasia) Apert Apert Syndrome Arnold Arnold - Chiari Malformation Arthogryposis Arthogryposis Multiplex Congenita Asphyxiating Jeune's Syndrome (Asphyxiating Thoracic Dystrophy) Ataxia Ataxia - Telangiectasia Ataxia Friedreich's Ataxia Auricular Goldenhar Syndrome (Auriculo Vertebral Syndrome) Bardet Bardet - Biedl Syndrome Barré Guillain - Barré Syndrome Bartter Bartter Syndrome Bassen Bassen - Kornzweig Syndrome Beckwith Beckwith - Wiedemann Syndrome Behçet Behçet Syndrome Blackfan Blackfan - Diamond Syndrome Biedl Bardet - Biedl Syndrome Biedl Lawrence - Moon - Biedl Syndrome Bloch Bloch - Sulzberger Syndrome Bowen Bowen Syndrome (Cerebrohepatorenal Syndrome) Bullae Cockayne - Touraine Syndrome (Dystrophic Epidermolysis Bullae) Butler Albright - Butler Syndrome (Primary Distal Renal Tubular Acidosis) Carpenter Carpenter Syndrome Central Core

104. –Ô–ŒF‘f•Ï«Ç‚𔺂¤‚±‚Æ‚ª‚ ‚éi‚Ü‚½‚́A”º
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  • yabetalipoproteinemiaz
    "abetalipoproteinemia" 18,300 Œ
    • Alagille ÇŒóŒQ
    "Alagille syndrome" 26,200 Œ
    "Alagille's syndrome" 472 Œ
    • Alport ÇŒóŒQ

    "Alport syndrome" 14200 Œ
    "Alport's syndrome" 3950 Œ
  • "Alstrom Hallgren syndrome" 277 Œ
    "Alström Hallgren syndrome" 9 Œ
    • Bassen-Kornzweig ÇŒóŒQ
    yBassen-Kornzweig syndromez [ƒoƒbƒZƒ“-ƒRƒ‹ƒ“ƒcƒ”ƒ@ƒCƒNÇŒóŒQ] "Bassen-Kornzweig syndrome" 1,810 Œ "Bassen-Kornzweig's syndrome" 3 Œ
    • Biemond ÇŒóŒQ
    "Biemond syndrome" 659 Œ
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