Descriptor
| Congenital Impairments | 20 |
| Exceptional Child Research | 17 |
| Medical Case Histories | 11 |
| Physical Disabilities | 11 |
| Infants | 9 |
| Genetics | 5 |
| Children | 4 |
| Clinical Diagnosis | 4 |
| Growth Patterns | 4 |
| Medical Research | 4 |
| Pregnancy | 4 |
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Source
| Journal of Pediatrics | 20 |
Author
| Smith, David W. | 2 |
| Benson, R. | 1 |
| Cohen, M. Michael, Jr. | 1 |
| Dacou-Voutetakis, C. | 1 |
| Daentl, Donna L. | 1 |
| Danks, David M. | 1 |
| Dudgeon, J. A. | 1 |
| Elders, M. Joycelyn | 1 |
| Fost, Norman | 1 |
| Gong, Bradley T. | 1 |
| Greenwood, Ronald D. | 1 |
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Publication Type
| Journal Articles | 1 |
| Reports - Evaluative | 1 |
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Peer reviewedDaentl, Donna L.; And Others – Journal of Pediatrics, 1975
Descriptors: Congenital Impairments, Etiology, Exceptional Child Research, Medical Case Histories
Peer reviewedPettifor, J. M.; Benson, R. – Journal of Pediatrics, 1975
Reported are case histories of three infants with congenital malformations (including defective formation of the nose and hands) associated with ingestion of oral anticoagulants during the first trimester of pregnancy. (CL)
Descriptors: Congenital Impairments, Exceptional Child Research, Infants, Medical Case Histories
Peer reviewedYang, Sheng-S.; And Others – Journal of Pediatrics, 1974
Descriptors: Clinical Diagnosis, Congenital Impairments, Exceptional Child Research, Infants
Peer reviewedDacou-Voutetakis, C.; And Others – Journal of Pediatrics, 1974
Descriptors: Biochemistry, Children, Congenital Impairments, Exceptional Child Research
Peer reviewedShahin, Bahman; And Others – Journal of Pediatrics, 1974
Descriptors: Biochemistry, Congenital Impairments, Exceptional Child Research, Infants
Peer reviewedDanks, David M.; And Others – Journal of Pediatrics, 1975
Examined were eight patients with cerebro-hepato-renal syndrome of Zellweger (associated with severe cerebral dysfunction, hypotonia and unusual appearance). (CL)
Descriptors: Congenital Impairments, Exceptional Child Research, Genetics, Incidence
Peer reviewedSteele, Mark W.; And Others – Journal of Pediatrics, 1974
Descriptors: Congenital Impairments, Diagnostic Tests, Exceptional Child Research, Genetics
Peer reviewedMabry, C. Charlton; And Others – Journal of Pediatrics, 1974
Descriptors: Case Studies, Clinical Diagnosis, Congenital Impairments, Exceptional Child Research
Peer reviewedElders, M. Joycelyn; And Others – Journal of Pediatrics, 1973
Laron's syndrome, characterized by severe dwarfism, high circulating levels of immunoreactive growth hormone, and failure to generate somatomedin after administration of human growth hormone, was studied in a boy 7 1/2 years of age. (MC)
Descriptors: Children, Congenital Impairments, Exceptional Child Research, Growth Patterns
Peer reviewedTemtamy, Samia A.; Miller, J. Daniel – Journal of Pediatrics, 1974
Descriptors: Classification, Congenital Impairments, Exceptional Child Research, Identification
Peer reviewedWaldman, A. Martin – Journal of Pediatrics, 1976
The author reviews some of his observations regarding the responsibility of the physician caring for the hopelessly ill child and presents the resolutions proposed in 1974 by the adhoc committee on Ethics and Survival. (SB)
Descriptors: Congenital Impairments, Decision Making, Ethics, Exceptional Child Education
Peer reviewedSmith, David W.; Gong, Bradley T. – Journal of Pediatrics, 1973
Descriptors: Congenital Impairments, Exceptional Child Research, Growth Patterns, Infants
Peer reviewedCohen, M. Michael, Jr.; And Others – Journal of Pediatrics, 1973
Presented were three case reports of patients, 8 to 18 years of age, who shared common features, such as obesity beginning in midchildhood, hypotonia, mental deficiency characteristic craniofacial appearance (antimongoloid slant, open mouth, or prominent central incisors), oral and ocular anomalies, and tapering extremities with narrow hands and…
Descriptors: Adolescents, Children, Congenital Impairments, Exceptional Child Research
Peer reviewedWaisbren, Susan E.; And Others – Journal of Pediatrics, 1983
Intelligence and speech-language development of eight children (3.6 to 11.6 years old) with classic galactosemia were assessed by standardized tests. Each of the children had delays of early speech difficulties, and all but one had language disorders in at least one area. Available from: Journal of Pediatrics, C.V. Mosby Co., 11830 Westline…
Descriptors: Children, Congenital Impairments, Intelligence Quotient, Language Handicaps
Peer reviewedDudgeon, J. A. – Journal of Pediatrics, 1975
Discussed are clinical manifestations, potential fetal damage, and prevention of congenital rubella. (CL)
Descriptors: Clinical Diagnosis, Congenital Impairments, Exceptional Child Research, Infants
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