scholarly journals Craniodiaphyseal Dysplasia

2020 ◽  
Author(s):  
Keyword(s):  
Craniodiaphyseal Dysplasia

Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia)

1978 ◽  
Vol 48 (1) ◽  
pp. 138-142 ◽  
Author(s):  
John K. Yen ◽  
Robert S. Bourke ◽  
A. John Popp ◽  
Carl R. Wirth
Keyword(s):  
Optic Nerve ◽  
Definitive Treatment ◽  
Content Type ◽  
X Ray ◽  
Metabolic Bone Disorder ◽  
Metabolic Bone ◽  
Bone Disorder ◽  
Craniodiaphyseal Dysplasia ◽  
Engelmann Disease ◽  
Fine Print

✓ In a patient with Camurati-Engelmann disease, orbital and optic nerve decompression resulted in improvement of papilledema. Subsequent x-ray films of the optic canals, however, revealed reconstitution of osseous optic canals bilaterally, and papilledema has returned in one eye. Definitive treatment of this dysplastic metabolic bone disorder rests in the control of rapid abnormal bone formation.

MR imaging features of craniodiaphyseal dysplasia

2003 ◽  
Vol 34 (2) ◽  
pp. 167-170 ◽  
Author(s):  
Franklin A. Marden ◽  
Franz J. Wippold
Keyword(s):  
Mr Imaging ◽  
Imaging Features ◽  
Craniodiaphyseal Dysplasia

Craniodiaphyseal Dysplasia (Mim 112860, 218300)

2012 ◽  
pp. 486-488
Author(s):  
Jürgen W. Spranger ◽  
Paula W. Brill ◽  
Gen Nishimura ◽  
Andrea Superti-Furga ◽  
Sheila Unger
Keyword(s):  
Clinical Findings ◽  
Differential Diagnoses ◽  
Radiographic Features ◽  
Craniodiaphyseal Dysplasia

Chapter 113 covers craniodiaphyseal dysplasia (MIM 112860, 218300), including major clinical findings, radiographic features, and differential diagnoses.

Craniodiaphyseal Dysplasia: A Case Report

1996 ◽  
Vol 35 (6) ◽  
pp. 983
Author(s):  
Gye Yeon Lim ◽  
Jeong Mi Park ◽  
Jae Mun Lee ◽  
Choon Yul Kim ◽  
Kyung Sub Shinn
Keyword(s):  
Case Report ◽  
Craniodiaphyseal Dysplasia

scholarly journals Craniodiaphyseal dysplasia, a very rare form of bone dysplasia

2020 ◽  
Vol 6 (1) ◽  
pp. 100137
Author(s):  
Bayar Ahmed Qasim ◽  
Ayad Ahmad Mohammed ◽  
Amer A. Balata ◽  
Sardar Hassan Arif ◽  
Laween Omar Musa
Keyword(s):  
Bone Dysplasia ◽  
Rare Form ◽  
Craniodiaphyseal Dysplasia

Macrocephaly and sclerosis of the tubular bones in an isolated patient: a mild case of craniodiaphyseal dysplasia?

2003 ◽  
Vol 12 (4) ◽  
pp. 245-250 ◽  
Author(s):  
Katrien Janssens ◽  
Elizabeth Thompson ◽  
Filip Vanhoenacker ◽  
Ravi Savarirayan ◽  
Lloyd Morris ◽  
...  
Keyword(s):  
Mild Case ◽  
Craniodiaphyseal Dysplasia ◽  
Tubular Bones

Craniodiaphyseal dysplasia: Evolution over a five-year period

1976 ◽  
Vol 1 (1) ◽  
pp. 47-53 ◽  
Author(s):  
A. S. Tucker ◽  
L. Klein ◽  
G. J. Antony
Keyword(s):  
Craniodiaphyseal Dysplasia
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