Литература. I. Виды зоба у детей
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24. Glorieux J, et al. Follow-up at age 5 and 7 years on mental development in children with hypothyroidism detected by Quebec screening program. J Pediatr 107: 913, 1985. 25. Glorieux J, et al. Useful parameters to predict the eventual mental outcome of hypothyroid children. Pediatr Res 24: 6, 1988. 26. Hanna CE, et al. Detection of congenital hypopituitary hypothyroidism: Ten years experience in the Northwest Regional Screening 91 Program. J Pediatr 109: 959, 1986. 27. Heyerdahl S, et al. Intellectual development in children with congenital hypothyroidism in relation to recommended thyroxine treatment. J Pediatr 118: 850, 1991. 28. Hollingsworth DR, Alexander NM. Amniotic fluid concentration of iodothyronines and thyrotropin do not reliably predict fetal thyroid status in pregnancies complicated by maternal thyroid disorders or anencephaly. J Clin Endocrinol Metab 57: 349, 1983. 29. Hollingsworth DR, Mabry CC. Congenital Graves' disease: Four familial cases with long-term follow-up and perspective. Am J Dis Child 130: 148, 1976. 30. Holtzman C, et al. Descriptive epidemiology of missed cases of phenylketonuria and congenital hypothyroidism. Pediatrics 78: 553, 1986. 31. Hughes VC, et al. The prevalence of thyroid dysfunction in mentally handicapped inpatients. J Ment Defic Res 26: 115, 1982. 32. Ibarrola N, et al. Effect of neonatal hypothyroidism on myelin protein gene expression. Abstracts of 19th Annual Meeting of the European Thyroid Association. Ann Endocrinol 52: 35, 1991. 33. Klein AH, et al. Improved prognosis in congenital hypothyroidism treated before age three months. J Pediatr 81: 912, 1972. 34. Klein RZ, et al. Prevalence of thyroid deficiency in pregnant women. Clin Endocrinol 35: 41, 1991. 35. Kohno H, et al. Pituitary cretinism in two sisters. Arch Dis Child 55: 725, 1980. 36. LaFranchi SH. Hypothyroidism, congenital and acquired. In SA Kaplan (ed), Clinical Pediatric and Adolescent Endocrinology. Philadelphia: Saunders, 1982. P. 87. 37. LaFranchi SH, et al. Neonatal hypothyroidism detected by the Northwest Regional Screening Program. Pediatrics 63: 180, 1979. 38. LaFranchi SH, et al. Screening program for congenital hypothyroidism with specimen collection at two time periods: Results of the Northwest Regional Screening Program. Pediatrics 76: 734, 1985. 39. Landau H, et al. Amniotic fluid, 3, 3'-5'-triiodothyronine in the detection of congenital hypothyroidism. J Clin Endocrinol Metab 50: 799, 1980. 40. Larsen PR, et al. Immunoassay of human TSH using dried blood samples. J Clin Endocrinol Metab 42: 987, 1976. 41. MacFaul R, Grant DB. Early detection of congenital hypothyroidism. Arch Dis Child 52: 87, 1977. 42. McLean RH, et al. Hypothyroidism in the congenital nephrotic syndrome. J Pediatr 101: 72, 1982. 43. Mandel SH, et al. Diminished thyroid-stimulating hormone secretion associated with neonatal thyrotoxicosis. J Pediatr 109: 662, 1986. 44. Matsuura N, et al. Familial neonatal transient hypothyroidism due to maternal TSH-binding inhibitor immunoglobulin. N Engl J Med 303: 738, 1980. 45. Miyai K, et al. Increased frequency of HLA-AW24 in congenital hypothyroidism in Japan (letter). N Engl J Med 303: 226, 1980. 46. Montoro M, et al. Successful outcome of pregnancy in women with hypothyroidism. Ann Intern Med 94: 31, 1981.
47. Muir A, et al. Thyroid scanning, ultrasound, and serum thyroglobulin in determining the origin of congenital hypothyroidism. Am J Dis Child 142: 214, 1988. 48. New England Congenital Hypothyroidism Collaborative. Characteristics of infantile hypothyroidism discovered on neonatal screening. J Pediatr 104: 539, 1984. 49. New England Congenital Hypothyroidism Collaborative. Neonatal hypothyroidism screening: Status of patients at 6 years of age. J Pediatr 107: 915, 1985. 50. New England Congenital Hypothyroidism Collaborative. Congenital concomitants of infantile hypothyroidism. J Pediatr 112: 244, 1988. 51. New England Congenital Hypothyroidism Collaborative. Elementary school performance of children with congenital hypothyroidism. J Pediatr 116: 27, 1990. 52. Penny R, et al. Congenital hypothyroidism in Spanish-surnamed infants in Southern California: Increased incidence and clustering of occurrence. Am J Dis Child 143: 640, 1989. 53. Perelman AA, et al. Intrauterine diagnosis and treatment of fetal goitrous hypothyroidism. J Clin Endocrinol Metab 71: 618, 1990. 54. Puymirat J, et al. Immunocytochemical localization of thyroid hormone receptors in the adult rat brain. Thyroid 1: 173, 1991. 55. Pyle I, Sontag LW. Variability in onset of ossification in epiphyses and short bones of the extremities. Am J Roentgenol 49: 795, 1943. 56. Ramsay I, et al. Thyrotoxicosis in pregnancy: Results of treatment by antithyroid drugs combined with T4. Clin Endocrinol 18: 73, 1983. 57. Rettig KR, et al. Discordance for congenital hypothyroidism in one monozygotic twin. Clin Pediatr 19: 63, 1980. 58. Richards GE, et al. Combined hypothyroidism and hypoparathyroidism in an infant after maternal 131I administration. J Pediatr 99: 141, 1981. 59. Rovet J, et al. Intellectual outcome in children with fetal hypothyroidism. J Pediatr 110: 700, 1987. 60. Rovet J, et al. Effect of thyroid hormone levels on temperament in infants with congenital hypothyroidism detected by screening of neonates. J Pediatr 114: 63, 1989. 61. Ruiz de Ona C, et al. Developmental changes in rat brain 5'-deiodinase and thyroid hormones during the fetal period: The effects of fetal hypothyroidism and maternal thyroid hormones. Pediatr Res 24: 588, 1988. 62. Thorpe-Beeston TG, et al. Maturation of the secretion of thyroid hormone and thyroid-stimulating hormone in the fetus. N Engl J Med 324: 532, 1991. 63. Vanderschueren-Lodeweyck M, et al. Sensorineural hearing loss in sporadic congenital hypothyroidism. Arch Dis Child 58: 419, 1983. 64. Vulsma T, et al. Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect or thyroid agenesis. N Engl J Med 321: 13, 1989. 65. Weichsel ME, Jr. Thyroid hormone replacement therapy in the perinatal period: Neurological considerations. J Pediatr 92: 1035, 1978. 66. Zakarija M, McKenzie JM. Pregnancy-associated changes in the thyroid-stimulating antibody of Graves' disease and the relationship to neonatal hypothyroidism. J Clin Endocrinol Metab 57: 1036, 1983. 67. Zakarija M, et al. Transient neonatal hypothyroidism: Characterization of maternal antibodies to the thyrotropin receptor. J Clin Endocrinol Metab 70: 1239, 1990. Глава 32. Болезни щитовидной железы у детей Н. Лавин Зоб Зоб — это видимое увеличение щитовидной железы. Зоб возникает при разных заболеваниях щитовидной железы и может сопровождаться клиническими проявлениями гипотиреоза либо тиреотоксикоза; нередко симптомы дисфункции щитовидной железы отсутствуют (эутиреоз). Таким образом, наличие зоба само по себе не позволяет установить причину заболевания. У большинства детей с зобом имеется эутиреоз. Частота зоба у детей составляет 4—5% и увеличивается с возрастом. У девочек зоб встречается чаще, чем у мальчиков (во всех возрастных группах). Существует несколько классификаций зоба; одна из них приведена в табл. 32. 1.
I. Виды зоба у детей А. Нетоксический зоб — приобретенное или врожденное заболевание щитовидной железы, не обусловленное тиреоидитом или опухолью, характеризующееся эутиреозом или гипотиреозом (по крайней мере, на ранней стадии). 1. Приобретенный нетоксический зоб (синонимы: простой зоб, простой нетоксический зоб, простой коллоидный зоб, ювенильный зоб). На долю этого заболевания приходится примерно 25% случаев увеличения щитовидной железы у детей. Клинических и биохимических признаков дисфункции железы нет. У девочек приобретенный нетоксический зоб встречается в 3—5 раз чаще, чем у мальчиков. Предполагают, что увеличение щитовидной железы при приобретенном нетоксическом зобе может быть обусловлено аутоантителами, стимулирующими пролиферацию клеток железы (но не секрецию тиреоидных гормонов). а. Осмотр. Железа равномерно увеличена, при пальпации гладкая, подвижная, безболезненная, нормальной консистенции.
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