نتایج جستجو برای: severe multiple synostosis

تعداد نتایج: 1061560  

2007
Felix Bierbrauer Martin Hellwig Felix J. Bierbrauer Martin F. Hellwig

We propose a new approach to the normative analysis of public-good provision in a large economy. Our analysis is based on a mechanism design approach that involves a requirement of coalition-proofness, as well as a requirement of robustness, so that the mechanism must not depend on specific assumptions about individual beliefs. Our main result shows that such a mechanism can condition only on t...

Journal: :Human molecular genetics 1997
G J Feldman D E Ward E Lajeunie-Renier D Saavedra N H Robin V Proud L J Robb V Der Kaloustian J C Carey M M Cohen V Cormier A Munnich E H Zackai A O Wilkie R A Price M Muenke

Craniofrontonasal syndrome (CFNS, OMIM 304110) is a distinctive genetic disorder whose main clinical manifestations include coronal synostosis, widely spaced eyes, clefting of the nasal tip and various skeletal anomalies. CFNS originally was thought to be transmitted as an autosomal dominant trait, but recent studies suggest that it is X-linked dominant, whereby all daughters of males are affec...

Journal: :Proceedings of the Royal Society of Medicine 1938

Journal: :Journal of maxillofacial and oral surgery 2009
P Hlongwa

Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the first year of life...

Journal: :British Journal of Haematology 2016

2008
J. Esparza J. Hinojosa I. García - Recuero A. Romance B. Pascual A. Martínez de Aragón

Objective. To review the results and complications of the surgical treatment of craniosynostosis in 283 consecutive patients treated between 1999 and 2007. Patients and methods. Our series consisted of 330 procedures performed in 283 patients diagnosed with scaphocephaly (n=155), trigonocephaly (n=50), anterior plagiocephaly (n=28), occipital plagiocephaly (n=1), non-syndromic multi-suture syno...

Journal: :The Journal of bone and joint surgery. British volume 2005
M Ramachandran K Lau D H A Jones

In five children, six forearms with a fixed pronation deformity secondary to congenital radioulnar synostosis were treated by a derotation osteotomy of the distal radius and the midshaft of the ulna. There were three boys and two girls with a mean age of 4.9 years (3.5 to 8.25) who were followed up for a mean of 29 months (18 to 43). The position of the forearm was improved from a mean pronatio...

Journal: :Cureus 2023

Introduction Loss of radius either due to trauma or infection results in a deformity resembling congenital radial club hand. This difficulty perform hand functions and cosmetic appearance is called acquired There are few case reports for the treatment this severe deformity, but there no proper guidelines management disease. From our experience, we decided provide Objectives To evaluate outcome ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید