Clinical genetics handbook /

Bibliographic Details
Other Authors: Robinson, Arthur, 1914-, Linden, Mary G.
Format: Book
Language:English
Published: Boston : Blackwell Scientific Publications, 1993.
Edition:Second edition.
Subjects:
Table of Contents:
  • Applied genetics
  • Genetic assessment and counseling by the primary care physician
  • Genetic counseling: principles and methods
  • Consanguinity
  • Reproductive failure: infertility, spontaneous abortion and stillbirth
  • Reproductive options
  • Prenatal diagnosis
  • Genetic screening
  • Disorders in clinical genetics
  • Mental retardation
  • Chromosome disorders
  • Autosomal chromosome syndromes
  • Down's syndrome
  • Sex chromosome anomalies
  • Fragile X syndrome
  • Neurologic disorders
  • Neural-tube defects: anencephaly/spina bifida
  • Hydrocephalus
  • Epilepsy
  • Tuberous sclerosis
  • Neurofibromatosis
  • Alzheimer's disease
  • Huntington's disease
  • Neuromuscular disorders
  • Genetic neuromuscular disorders
  • Muscle disorders
  • Genetic muscle disorders: dystrophies, myotonias and myopathies
  • Hematologic disorders
  • Heritable clotting disorders
  • Sicke-cell anemia
  • Thalasemias
  • Cardiovascular disorders
  • Predisposition to coronary artery disease
  • Hypertension
  • Congenital heart defects
  • Skeletal system disorders
  • Short stature
  • Congenital limb defects.
  • (cont) Respiratory system disorders
  • Cystic fibrosis
  • α₁-antitrypsin deficiency
  • Urogenital system disorders
  • Cystic kidney disease
  • Ambiguous genitalia and hermaphroditism
  • Disorders of other specific systems
  • Genetic disorders of the immune system
  • Hereditary visual disorders
  • Hereditary hearing loss
  • Genetic disorders of the skin
  • Hereditary disorders of connective tissue
  • Metabolic disease
  • Classification of inborn errors of metabolism
  • Tay-Sachs disease
  • Wilson's disease
  • Diabetes mellitus
  • Phenylketonuria
  • Cancer
  • Hereditary cancers
  • Familial forms of breast cancer
  • Genetic forms of colon cancer
  • Psychiatric disorders
  • Alcoholism and fetal alcohol syndrome
  • Multiple congenital anomalies
  • Syndromes/symptom complexes
  • Teratogenesis
  • Isolated congenital anomalies
  • Cleft lip and/or cleft palate
  • Other isolated birth defects
  • Pharmacogenetics
  • Genetic problems in anesthesia
  • Glucose-6-phosphate dehydrogenase deficiency (drug-induced hemolytic anemia)
  • Porphyria.