Hyperimmunoglobulinemia E syndrome: association with osteoporosis and recurrent fractures.

Radiology ◽  
1985 ◽  
Vol 156 (2) ◽  
pp. 362-362 ◽  
Author(s):  
S G Kirchner ◽  
C J Sivit ◽  
P F Wright
Keyword(s):  
Hyperimmunoglobulinemia E ◽  
Syndrome Association

Does hyperimmunoglobulinemia-E protect tropical populations from allergic disease?

1983 ◽  
Vol 71 (2) ◽  
pp. 184-188 ◽  
Author(s):  
J LARRICK ◽  
C BUCKLEYIII ◽  
C MACHAMER ◽  
G SCHLAGEL ◽  
J YOST ◽  
...  
Keyword(s):  
Allergic Disease ◽  
Hyperimmunoglobulinemia E

scholarly journals Pediatric loss of control eating syndrome: Association with attention-deficit/hyperactivity disorder and impulsivity

2015 ◽  
Vol 48 (6) ◽  
pp. 580-588 ◽  
Author(s):  
Shauna P. Reinblatt ◽  
E. Mark Mahone ◽  
Marian Tanofsky-Kraff ◽  
Angela E. Lee-Winn ◽  
Gayane Yenokyan ◽  
...  
Keyword(s):  
Attention Deficit Hyperactivity Disorder ◽  
Attention Deficit ◽  
Loss Of Control ◽  
Loss Of Control Eating ◽  
Hyperactivity Disorder ◽  
Syndrome Association

Vernal Conjunctivitis in the Hyperimmunoglobulinemia E Syndrome

Ophthalmology ◽  
1984 ◽  
Vol 91 (10) ◽  
pp. 1213-1216 ◽  
Author(s):  
Salim I. Butrus ◽  
Donald Y.M. Leung ◽  
Steven Gellis ◽  
Jules Baum ◽  
Kenneth R. Kenyon ◽  
...  
Keyword(s):  
Hyperimmunoglobulinemia E ◽  
Vernal Conjunctivitis

Ellis-van Creveld Syndrome and Dyserythropoiesis

2005 ◽  
Vol 129 (5) ◽  
pp. 680-682 ◽  
Author(s):  
Deven Scurlock ◽  
Daniel Ostler ◽  
Andy Nguyen ◽  
Amer Wahed
Keyword(s):  
Myelodysplastic Syndrome ◽  
Autosomal Recessive ◽  
Ectodermal Dysplasia ◽  
Case Reports ◽  
Clinical Manifestations ◽  
Autosomal Recessive Disorder ◽  
Clinical Findings ◽  
Cardiac Defects ◽  
Ellis Van Creveld Syndrome ◽  
Syndrome Association

Abstract Ellis-van Creveld (EVC) syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder characterized by a variable spectrum of clinical findings. Classical EVC syndrome comprises a tetrad of clinical manifestations of chondrodystrophy, polydactyly, ectodermal dysplasia, and cardiac defects. In several case reports, dysplasia involving other organs has also been identified. Hematologic abnormalities have been rarely reported in patients with EVC syndrome. Here, we report a case of a 3-year-old Hispanic boy with EVC syndrome and marked dyserythropoiesis. The dyserythropoiesis may be part of an isolated myelodysplastic change or a primary myelodysplastic syndrome and likely represents an unusual EVC syndrome association. To our knowledge, this association has not been previously reported.

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