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Quoted phrase not found in phrase index: "Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities"
Page 1
Inflammatory Arthritis as a Possible Feature of Coffin-Siris Syndrome.
Pediatrics. 2019 Jul;144(1):e20181741. doi: 10.1542/peds.2018-1741.
Pediatrics. 2019.
PMID: 31243159
With synovial biopsy, we confirmed a chronic inflammatory synovitis. Brain MRI revealed dysgenesis of the corpus callosum. Treatment with methotrexate and, subsequently, etanercept led to significant clinical improvement. ...We propose that some patients with CSS ma …
With synovial biopsy, we confirmed a chronic inflammatory synovitis. Brain MRI revealed dysgenesis of the corpus callosum. Treatment …
A fourth case of Feingold syndrome type 2: psychiatric presentation and management.
Ganjavi H, Siu VM, Speevak M, MacDonald PA.
Ganjavi H, et al.
BMJ Case Rep. 2014 Nov 12;2014:bcr2014207501. doi: 10.1136/bcr-2014-207501.
BMJ Case Rep. 2014.
PMID: 25391829
Free PMC article.
Review.
Feingold syndrome (FGLDS1) is an autosomal dominant disorder caused by mutations in the MYCN oncogene on the short arm of chromosome 2 (2p24.1). ...In 2011, individuals sharing the skeletal abnormalities of FGLDS1 but lacking mutations in MYCN, were found to …
Feingold syndrome (FGLDS1) is an autosomal dominant disorder caused by mutations in the MYCN oncogene on the short arm of chromosome …
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