Engelmann's disease with optic atrophy

Engelman-Camurati disease is a rare Diaphyseal dysplasia, characterized by endosteal and periostal thickness of cortex of shaft of tubular bone sparing metaphysis and epiphysis. The bone of the hand, feet, ribs, scapulae and pubis are not affected.

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Bibliographische Detailangaben
Veröffentlicht in:	Indian journal of pediatrics 2002-09, Vol.69 (9), p.823-824
Hauptverfasser:	SONI, J. P, GUPTA, B. D, SONI, M, MUND, V, ANEJA, Rajesh
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Camurati-Engelmann Syndrome - complications Camurati-Engelmann Syndrome - diagnosis Diseases of visual field, optic nerve, optic chiasma and optic tracts Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes Follow-Up Studies Humans India Infant Male Medical sciences Nervous system (semeiology, syndromes) Neurology Ophthalmology Optic Atrophy - complications Optic Atrophy - diagnosis Risk Assessment
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Beschreibung
Zusammenfassung:	Engelman-Camurati disease is a rare Diaphyseal dysplasia, characterized by endosteal and periostal thickness of cortex of shaft of tubular bone sparing metaphysis and epiphysis. The bone of the hand, feet, ribs, scapulae and pubis are not affected.
ISSN:	0019-5456 0973-7693
DOI:	10.1007/BF02723700