About the Book
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 91. Chapters: Ciliopathy, Cytoskeletal defects, Mitochondrial diseases, Nucleus diseases, Peroxisomal disorders, Scleroprotein and ECM diseases, Joubert syndrome, Marfan syndrome, Charcot-Marie-Tooth disease, Parkinson's disease, Amyotrophic lateral sclerosis, Hypertrophic cardiomyopathy, Usher syndrome, Hereditary spastic paraplegia, Treacher-Collins syndrome, Long QT syndrome, Laminopathy, Dilated cardiomyopathy, Leber's hereditary optic neuropathy, Kearns-Sayre syndrome, Spinocerebellar ataxia, Primary ciliary dyskinesia, Bardet-Biedl syndrome, Survival motor neuron spinal muscular atrophy, Friedreich's ataxia, Tauopathy, Caroli disease, Polycystic kidney disease, Chronic progressive external ophthalmoplegia, Nonsyndromic deafness, MELAS syndrome, Wiskott-Aldrich syndrome, Hereditary spherocytosis, Epidermolytic hyperkeratosis, Cornelia de Lange Syndrome, Alstrom syndrome, Barraquer-Simons syndrome, Meckel syndrome, Wolfram syndrome, Alagille syndrome, Ichthyosis bullosa of Siemens, Alexander disease, Zellweger syndrome, Leigh's disease, Danon disease, Pelger-Huet anomaly, Senior-Loken syndrome, Autosomal recessive polycystic kidney, MERRF syndrome, Ichthyosis hystrix, Neuropathy, ataxia, and retinitis pigmentosa, White sponge nevus, Revesz syndrome, Monilethrix, Osteopoikilosis, Giant axonal neuropathy, Orofaciodigital syndrome 1, Weill-Marchesani syndrome, Mitochondrial myopathy, May-Hegglin anomaly, Steatocystoma multiplex, Buschke-Ollendorff syndrome, Mitochondrial neurogastrointestinal encephalopathy syndrome, Keratin disease, Epidermolysis bullosa simplex, Congenital contractural arachnodactyly, Asphyxiating thoracic dysplasia, Pearson syndrome, Striate palmoplantar keratoderma, Pseudoachondroplasia, Meesmann juvenile epithelial corneal dystrophy, Diabetes mellitus and deafness, Junctional epidermolysis...
