An unusual case of pycnodysostosis

Archives of Disease in Childhood

Volumn 63, Issue 5, 1988, Pages 558-559

  Kumar, R ^a,b   Misra, P K ^a   Singhal, R ^a  

^a KING GEORGE'S MEDICAL UNIVERSITY   (India)

^b Aliganj   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALBERS SCHOENBERG DISEASE; ANEMIA; CASE REPORT; CONGENITAL MALFORMATION; DYSOSTOSIS; HUMAN; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; PYKNODYSOSTOSIS;

ANEMIA, MYELOPHTHISIC; CASE REPORT; CHILD; DYSOSTOSES; HEPATOMEGALY; HUMAN; MALE; OSTEOPETROSIS; SPLENOMEGALY;

EID: 0023942146     PISSN: 00039888     EISSN: None     Source Type: Journal    
DOI: 10.1136/adc.63.5.558     Document Type: Article

References (5)

1. Maroteaux, P. The osteochondrodysplasias 1979 116 diseases of children
2. Baker, R.K.; Wallach, S.; Tashjian, A.H. Plasma calcitonin in pycnodysostosis: intermittently high basal levels and exaggerated response to calcium and glucagon infusion Journal of Clinical Endocrinology 1973 10.1210/jcem-37-1-46 37 46
3. P, Sarn Sethsiri; OK, Hitt; EJ, Eyring; HM, Frost Tetracycline based study of bone dynamics in pycnodysostosis Clin Orthop 1971 10.1097/00003086-197101000-00035 74 301
4. Elmore, S.M.; Nance, W.E.; McGee, B.J. Pycnodysostosis with a familial chromosome anomaly Am J Med 1966 10.1016/0002-9343(66)90108-2 40 273
5. Kozlwski, K.; Yu, J.S. Pycnodysostosis: a variant form with visceral manifestations Arch Dis Child 1972 10.1136/adc.47.255.804 47 804