Neurocutaneous Diseases. A Practical Approach

Content: 
Front Matter, Page iii
Copyright, Page iv
Contributing Authors, Pages vii-viii
Foreword, Page ix, Raymond D. Adams
Preface, Pages xi-xii, M.R.G.
Chapter 1 - Genetic Principles, Pages 1-8, WILLIAM G. JOHNSON
Chapter 2 - Neurofibromatosis, Pages 11-29, VINCENT M. RICCARDI
Chapter 3 - Tuberous Sclerosis, Pages 30-52, MANUEL R. GOMEZ
Chapter 4 - Von Hippel–Lindau Disease, Pages 53-66, VIRGINIA V. MICHELS
Chapter 5 - Nevoid Basal Cell Carcinoma Syndrome, Pages 67-79, ROBERT J. GORLIN
Chapter 6 - Lentiginosis-Deafness-Cardiopathy Syndrome, Pages 80-84, DONALD J. HAGLER
Chapter 7 - Hypomelanosis of Ito, Pages 85-90, IGNACIO PASCUAL-CASTROVEIJO
Chapter 8 - Other Autosomal Dominant Diseases, Page 91, MANUEL R. GOMEZ
Chapter 9 - Ataxia-Telangiectasia, Pages 95-117, ELENA BODER
Chapter 10 - Xeroderma Pigmentosum, Pages 118-127, JAY H. ROBBINS
Chapter 11 - Cockayne's Syndrome, Pages 128-135, DONALD ZIMMERMAN
Chapter 12 - Rothmund–Thomson Syndrome, Pages 136-142, ROBERTA A. PAGON
Chapter 13 - Fucosidosis, Pages 143-154, MICHEL PHILIPPART
Chapter 14 - Phenylketonuria and Hyperphenylalaninemia, Pages 155-170, VIRGINIA V. MICHELS
Chapter 15 - Homocystinuria due to Cystathionine Synthase Deficiency, Pages 171-181, PAUL R. DYKEN
Chapter 16 - Citrullinemia and Arginosuccinicaciduria, Pages 182-186, STUART B. BROWN
Chapter 17 - Biotin-responsive Multiple Carboxylase Deficiency, Pages 187-194, HERBERT M. SWICK
Chapter 18 - Cerebrotendinous Xanthomatosis, Pages 195-199, JAMES R. SCHIMSCHOCK
Chapter 19 - Familial Dysautonomia, Pages 200-208, FELICIA B. AXELROD, JOHN PEARSON
Chapter 20 - Chediak–Higashi Syndrome, Pages 209-213, PHILIP VAN HALE
Chapter 21 - Neuroichthyosis, Pages 214-218, RAMON RUIZ-MALDONADO
Chapter 22 - Sjögren–Larsson Syndrome, Pages 219-224, ENRIQUE CHAVES-CARBALLO
Chapter 23 - Refsum's Disease, Pages 225-235, SIGVALD REFSUM, ODDVAR STOKKE
Chapter 24 - Giant Axonal Neuropathy, Pages 236-240, BRUCE O. BERG
Chapter 25 - Werner's Syndrome, Pages 241-246, MAKOTO GOTO
Chapter 26 - Progeria, Pages 247-253, HANS-RUDOLF WIEDEMANN
Chapter 27 - Neuroectodermal Melanolysosomal Disease, Pages 254-260, B. RAFAEL ELEJALDE, MARIA MERCEDES DE ELEJALDE
Chapter 28 - Ruvalcaba–Myhre Syndrome, Pages 261-262, DONALD ZIMMERMAN
Chapter 29 - Fabry–Anderson Disease, Pages 265-272, MICHEL PHILIPPART
Chapter 30 - Adrenoleukodystrophy, Pages 273-283, BRIAN P. O'NEILL
Chapter 31 - Kinky Hair Disease, Pages 284-292, JOHN H. MENKES
Chapter 32 - Incontinentia Pigmenti, Pages 293-300, N. PAUL ROSMAN
Chapter 33 - A Syndrome of Anosmia, Ichthyosis, and Hypogonadism with Steroid Sulfatase and Arylsulfatase C Deficiencies, Pages 301-304, NOBUHIKO SUNOHARA, EIJIRO SATOYOSHI
Chapter 34 - Coffin–Siris Syndrome, Pages 307-310, WILLIAM A. DE BASSIO
Chapter 35 - Albinism, Pages 311-325, RICHARD A. KING
Chapter 36 - Neurocutaneous Melanosis, Pages 329-334, IGNACIO PASCUAL-CASTROVIEJO
Chapter 37 - Linear Sebaceous Nevus, Pages 335-344, ARTHUR L. PRENSKY
Chapter 38 - Cerebello-Trigemino-Dermal Dysplasia, Pages 345-348, MANUEL R. GOMEZ
Chapter 39 - Encephalo-Cranio-Cutaneous Lipomatosis, Pages 349-355, MARVIN A. FISHMAN
Chapter 40 - Sturge–Weber Syndrome, Pages 356-367, MANUEL R. GOMEZ, ELIZABETH M. BEBIN
Chapter 41 - Klippel–Trenaunay Syndrome, Pages 368-375, GUNNAR B. STICKLER
Chapter 42 - Wyburn–Mason Syndrome, Pages 376-380, BRIAN R. YOUNGE
Chapter 43 - Maffucci's Syndrome, Pages 381-383, W. EDWIN DODSON
Chapter 44 - Rare and Questionable Vascular Neurocutaneous Diseases, Pages 384-386, MANUEL R. GOMEZ
Index, Pages 387-401