Letter: Rickets in neonatal hepatitis.

Neonatal rickets in one of identical twins.

Juberg R C, Hayward J R. A new familial syndrome of oral, cranial, and digital anomalies. J Pediatr 1969; 74: 755-62. 2 Nevin N C, Henry P, Thomas P T S. A case of the orocraniodigital (Juberg-Hayward) syndrome. J Med Genet 1981; 18: 478-80. 3 Savage D C L, Swift P G F, Johnston P G B, Goldie D J, Murphy D. Combined test of anterior pituitary function in children. Arch Dis Child 1978; 53: 301-4...

Neonatal rickets in Asian immigrant population.

Neonatal rickets. Histopathology and quantitative bone changes.

Ribs from 3 preterm infants, who had died after prolonged intravenous feeding and artificial ventilation, were examined histologically and assessed for the degree of osteomalacia and osteoporosis in cancellous bone of the shaft. A grid counting technique was used. Osteomalacia was noted in all 3 cases but to a lesser degree than in classical vitamin D-deficient controls. Osteoporosis was pronou...

Hepatitis antigen and -fetoprotein in neonatal hepatitis.

Ladd, W. E. (1932). Congenital obstruction of the duodenum in children. New England Journal of Medicine, 206, 277. Rowe, M. I., Buckner, D., and Clatworthy, H. W., Jr. (1968). Wind sock web of the duodenum. AmericanJournal of Surgery, 116,444. Snyder, W. H., and Chafflin, L. (1954). Embryology and pathology of the intestinal tract: presentation of 40 cases of malrotation. Annals of Surgery, 140...

Diagnostic dilemma: osteopetrosis with superimposed rickets causing neonatal hypocalcemia.

Osteopetrosis is a rare genetic condition of reduced osteoclastic bone resorption which causes defective bone remodeling and skeletal sclerosis during growth, having effects on many organs and tissues. Mutation of T-cell immune regulator 1 (TCRG1) gene is the most common genetic defect leading to osteopetrosis, with poor prognosis. The autosomal recessive form presents in the infantile period (...