About the Book
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 88. Chapters: Von Hippel-Lindau disease, Say-Meyer syndrome, Hereditary hemorrhagic telangiectasia, Tuberous sclerosis, Treacher-Collins syndrome, DiGeorge syndrome, Von Willebrand disease, Porphyria cutanea tarda, Multiple endocrine neoplasia, Spinocerebellar ataxia, Myotonic dystrophy, Hereditary elliptocytosis, Noonan syndrome, Multiple endocrine neoplasia type 2b, Stickler syndrome, Multiple endocrine neoplasia type 1, Keratolytic winter erythema, Variegate porphyria, Flynn-Aird syndrome, Timothy syndrome, Axenfeld syndrome, Boomerang dysplasia, Marshall syndrome, Albright's hereditary osteodystrophy, Felty's syndrome, Short QT syndrome, Nail-patella syndrome, PAPA syndrome, Holt-Oram syndrome, Fibromuscular dysplasia, Transthyretin-related hereditary amyloidosis, Darier's disease, Kostmann syndrome, Liddle's syndrome, Pallister-Hall syndrome, Pelger-Huet anomaly, MOMO syndrome, Spondyloepiphyseal dysplasia congenita, Gardner's syndrome, Hay-Wells syndrome, Vitelliform macular dystrophy, Popliteal pterygium syndrome, Familial atrial fibrillation, Miller-Dieker syndrome, Pachyonychia congenita, Hajdu-Cheney syndrome, Jackson-Weiss syndrome, Central core disease, Greig cephalopolysyndactyly syndrome, White sponge nevus, Zimmermann-Laband syndrome, WHIM syndrome, Larsen syndrome, Romano-Ward syndrome, Monilethrix, Spondyloepimetaphyseal dysplasia, Strudwick type, Van der Woude syndrome, De Vivo disease, Oculopharyngeal muscular dystrophy, Tietz syndrome, Rosselli-Gulienetti syndrome, Naegeli-Franceschetti-Jadassohn syndrome, Langer-Giedion syndrome, Kniest dysplasia, Bethlem myopathy, Dermatopathia pigmentosa reticularis, Collagenopathy, types II and XI, Worth syndrome, Spondyloperipheral dysplasia, Congenital stromal corneal dystrophy, Gray platelet syndrome, Hereditary mucoepithelial dysplasia, Granular corneal dystrophy type ...
