The early diagnosis of congenital abnormalities / R.W. Smithells.

  • Smithells, R. W. (Richard Worthington)
Date:
1963
Catalogue details

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

Credit: The early diagnosis of congenital abnormalities / R.W. Smithells. Source: Wellcome Collection.

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    INDEX 195 Macrocephaly, 48 Macroglossia, 77, 121 Malformations, prenatal diag¬ nosis, 1-25 Malnutrition, maternal, and mal¬ formations, 10 Mandibulofacial dysostosis, 65 genetics, 173 Marfan's syndrome, 96 Masculinization, 11, 86 Maternal age and parity, 12- 13 Meckel's diverticulum, 34, 145 Meconium, 89 failure to pass, 92-4 ileus, 145; 146 peritonitis, 145; 148 plugs, 92,149 Melaena, 95 Meningocele cranial, 27, 51 spinal, 68 Meningoencephalocele, 27, 51 Meningomyelocele, 69 genetics, 177 prenatal diagnosis, 17; 18 Metabolic functions, examination of, 109-16 Methaemoglobinaemia, 131-2 Microcephaly, 48-9 genetics, 173 Micrognathia, 65,119-21, 132 Microphthalmos, 58 Microtia, 65 Micturition, 90 foetal, 6, 34 Möbius's syndrome, 132, 133 Mongolism, 13, 54-7, 133 genetics, 174-6 and maternal age, 13 Mosaics, chromosomal, 89, 174 Mouth, examination of, 76-7 Mucoviscidosis, 3, 95-6 genetics, 171 Murmurs, cardiac, 24, 72-4 Muscles, aplasia, 77,104-5 Muscular atrophy, infantile spinal, 133 genetics, 176 Muscular dystrophy, 133 genetics, 176 Myasthenia gravis, 133-4 Myelomeningocele, 17, 69 genetics, 177 prenatal diagnosis, 17; 18 Myocardium, disorders of, 128 Myopia, 59 Naevi giant, with thrombocytopaenia,. 109 pigmented, 107; 108 vascular, 107 Neck, examination of, 71 Nephrogenic diabetes insipidus,25 Niemann-Pick disease, 176 Nipple, absence of, 105 Non-disjunction, chromosomal,. 13,174-6 Nucleara genesis {see Möbius's syndrome) — chromatin, 87 — sex, 87 Obstruction, intestinal, 134-49 Oedema in gonadal dysgenesis, 89 Oesophageal atresia, 136-40; 137^ 139, 141 and polyhydramnios, 6 Oesophagotracheal fistula, 131, 138; 137 Oligohydramnios, 6-8 ; 7 Omphalocele (see Exomphalos) Ortolani's test, 101-3 Ossification centres at birth, 114 Osteochondrodystrophy, 97 Osteogenesis imperfecta, 46, 97 genetics, 176 prenatal diagnosis, 19 Ovarian agenesis {see Gonadal dysgenesis) Oxycephaly, 50