نتایج جستجو برای: severe multiple synostosis

تعداد نتایج: 1061560  

2014
Myung-Sang Moon Sung-Soo Kim Min-Geun Yoon Young Hoon Seo Bong-Jin Lee Hanlim Moon Sung-Sim Kim

STUDY DESIGN A prospective radiographic study of cervical spine with congenital monosegment fusion. PURPOSE To evaluate the effect of cervical synostosis on adjacent segments and the vertebral morphology. OVERVIEW OF LITERATURE There are numerous clinical studies of adjacent segment disease (ASD) after monosegment surgical fusion. However, there was no report on ASD in the cervical spine wi...

Journal: :Our Dermatology Online 2022

Apert syndrome is a rare which presents with craniosynostosis, severe syndactyly, and dysmorphic facial features. It mainly caused by new mutation in fibroblast growth factor receptor-2 gene. Up-regulation of this gene results bone fusion nuclear deficiency the transcription FoxO1 key pathogenesis acne. We present herein 19-year-old man nodulocystic acne associated acrocephaly, prominent forehe...

Journal: :Congenital anomalies 2003
Yumiko Kanauchi Yasuteru Muragaki Toshihiko Ogino Masatoshi Takahara Hiroyuki Tsuchida Daisuke Ishigaki

Most cases of Apert syndrome are due to S252W or P253R mutations in the fibroblast growth factor receptor 2 (FGFR2) gene. Differences in the effects of S252W and P253R mutations on the clinical features of Apert syndrome have been studied, but little is known about the type of FGFR2 mutation in Apert syndrome with humeroradial synostosis. To study a correlation between the FGFR2 mutations and t...

2016
Kamlesh B. Patel Dennis C. Nguyen Gary B. Skolnick Sybill D. Naidoo Matthew D. Smyth

1. Carlsen NL, Krasilnikoff PA, Eiken M. Premature cranial synostosis in X-linked hypophosphatemic rickets: possible precipitation by 1-alpha-OH-cholecalciferol intoxication. Acta Paediatr Scand 73(1):149–54, 1984 2. Currarino G. Sagittal synostosis in X-linked hypophosphatemic rickets and related diseases. Pediatr Radiol 37(8):805–12, 2007 3. Freudlsperger C, Hoffmann J, Castrillon-Oberndorfer...

Journal: :Child's Nervous System 2012

Journal: :Human molecular genetics 2006
Amy E Merrill Elena G Bochukova Sean M Brugger Mamoru Ishii Daniela T Pilz Steven A Wall Karen M Lyons Andrew O M Wilkie Robert E Maxson

Boundaries between cellular compartments often serve as signaling interfaces during embryogenesis. The coronal suture is a major growth center of the skull vault and develops at a boundary between cells derived from neural crest and mesodermal origin, forming the frontal and parietal bones, respectively. Premature fusion of these bones, termed coronal synostosis, is a common human developmental...

2010
Nikolaos K. Sferopoulos

The incidence of synostosis of the proximal tibiofibular joint (TFJ) was assessed among 1029 patients examined for osteoarthritis of the knee in a 4-year period. Radiographic evidence of a synostosis of the proximal TFJ was demonstrated in 3 knees (3 patients). The synostosis appeared incidental and was not the cause of symptoms in any of them. These patients were further examined with MRI and/...

Journal: :The Journal of bone and joint surgery. British volume 1996
G H Albers A F de Kort P R Middendorf C N van Dijk

Over an eight-year period up to 1983, a total of 322 consecutive patients had operations for ankle fractures; 176 were Weber type B and 128 type C. We were able to review 230 of these patients after a mean follow-up of six years (1 to 11) including 128 with Weber B and 102 with Weber C fractures. We used an ankle score which combined symptoms and clinical and radiological findings, with a maxim...

Journal: :Case Reports 2010

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید