Handbook of congenital malformations / edited by Alan Rubin.

Date:
1967
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Handbook of congenital malformations / edited by Alan Rubin. Source: Wellcome Collection.

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    INDEX Deafness {Continued) nerve, hereditary nephritis and, with urticaria and amyloidosis, 235 heredodegenerative, 234 neurofibromatosis and, localized, 234 piebaldness and, 232 subcortical encephalopathy and, 234 perceptive, in cervico-oculo-acoustic syndrome, 230 quinine and, 369 sporadic goiter and, 244 white forelock and, 227 De Lange syndrome, 117 Dental anomalies, 103-156 in cleidocranial dysostosis, 57 in dysplasia oculodentodigitalis syn¬ drome, 265 in ectodermal dysplasia, hypohi- drotic, 265 in Ellis-Van Creveld syndrome, 62 in focal dermal hypoplasia syn¬ drome, 271 Dentin dysplasia of, 119 enamel and, hypoplasia and intrinsic staining of, 124, 126 hereditary opalescent, 118 Dentinogenesis imperfecta, without bone disease, 118 Dentition. See Teeth. Dermatitis, in Cockayne's disease, 262 in Danbolt-Closs syndrome, 258 Dermatomegaly, 263 Dermoids. See Cyst(s), dermoid. Dermolipoma, 186 Dextrocardia, 26 Diabetes, hereditary, with nephritis, epilepsy, nerve deafness, and men¬ tal retardation, 235 maternal, sacral aplasia and, 368 Diaphragm, congenital eventration of, 158 congenital relaxation of, 158 hernia of, 159 Diaphyses, malformations of, 62, 63 Diastematomyelia, 91 Dicvmiarol, fetal bleeding and, 367 Diethylstilbestrol, as teratogenic agent, 367 Digestive system, anomalies of, 1-14 Digits. See also Finger(s) and Toe(s). clubbing of, in cardiovascular anom¬ aly, 21 fusion of, 83 in focal dermal hypoplasia syn¬ drome, 271 in Léri's pleonosteosis, 69 Digits {Continued) in oculodentodigitalis syndrome, 265 supernumerary, 78 tongue and, aplasia of, 104 Diphallus, 326 Diplegia, facial, 128 oculofacial, 128 Disease. See also proper names, e.g., Witkop's disease. cystic, of liver and kidney, 322 of renal pyramids, 320 cytomegalic inclusion, 353 fibrocystic, of pancreas, 12 glycogen storage, 28 heart. See Heart disease. hyperostotic bone, hereditary gen¬ eralized, 133 labyrinthine, in identical twins, 241 of kidney, polycystic, 318, 319 of pancreas, fibrocystic, 12 Dislocation, congenital. See Subluxa¬ tion, congenital. Distichiasis, 186 Diverticulum (a) giant, 7 Meckel's, 8 of bladder, 297 of esophagus, 4 of left ventricle, 30 of pharynx, 256 of ureter, 335 of urethra, 339 Double bladder, 299 Double cervix, 347 Double larynx, 252 Double lip, 139 Double tongue, 148 Double ureter, 336 Double urethra, 340 Double uterus, 347 Double vagina, 350 Doughnut kidney, 315 Down's syndrome, 96 Drugs, congenital malformations and, 365-371 Duane's retraction syndrome, 187 Duplication of alimentary tract, 4, 7 Dupuytren's contracture, 58 Dwarf. See also Dwarfism. achondroplastic, 51 Amsterdam, 117 bird-headed, of Seckel, 110 pituitary, 47 Dwarfism. See also Dwarf. in dysplasia epiphysialis multiplex, 59 in dysplasia epiphysialis punctata, 60 382