نتایج جستجو برای: limb defect

تعداد نتایج: 165469  

Journal: :The Turkish journal of pediatrics 2017
Burak Ardıçlı Ayşe Karaman Ahmet Özyazıcı Ayşegül Zenciroğlu Nurullah Okumuş

Ardıçlı B, Karaman A, Özyazıcı A, Zenciroğlu A, Okumuş N. Isolated thoracoschisis: Case report. Turk J Pediatr 2017; 59: 217-220. Thoracoschisis is a rare congenital anomaly that refers to a congenital fissure of the chest wall. It is frequently accompanied with other congenital defects of the limbs and the abdominal wall as part of the limb-body wall complex, which is exencephaly/encephalocele...

Journal: :Journal of medical genetics 1992
J R Ward C Saad de Owens I A Sierra

Two sibs are reported with upper limb defect, developmental delay, central hearing loss, unilateral poorly developed antihelix, and bilateral choroid coloboma. The inheritance is probably autosomal recessive.

Journal: :iranian journal of medical sciences 0
binoy shankar department of neonatology and paediatric medicine, pgimer, dr. rml hospital, new delhi, india euden bhutia department of neonatology and paediatric medicine, pgimer, dr. rml hospital, new delhi, india dinesh kumar department of neonatology and paediatric medicine, pgimer, dr. rml hospital, new delhi, india sunil kishore department of neonatology and paediatric medicine, pgimer, dr. rml hospital, new delhi, india shakti pad das department of neonatology and paediatric medicine, pgimer, dr. rml hospital, new delhi, india

holt-oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are bilateral and asymmetrical. they range from clinodactyly, absent or digitalised thumb, hypoplastic...

Journal: :British Journal of Surgery 2021

Abstract 30 year old male, who had been hit at 90mph whilst on a motorbike sustaining femoral, tibial and right foot open fractures. He underwent an reduction internal fixation (ORIF) of his lateral femoral condyle, retrograde nail, ORIF the tibia. 2 separate free flaps (a chimera scapular/parascapular antero-lateral thigh-ALT) to lower leg, split skin grafting remainder limb. Upon regular post...

Journal: :The International journal of developmental biology 2002
Yukari Yada Shigeru Makino Sadao Chigusa-Ishiwa Toshihiko Shiroishi

Pattern formation along the anterior-posterior axis of the vertebrate limb is established upon activation of Sonic Hedgehog (SHH) in the zone of polarizing activity (ZPA). Since many mouse mutants with preaxial polydactyly show ectopic expression of Shh at the anterior margin of the limb buds, it has been thought to be a primary defect caused by these mutations. We show here that the mouse muta...

Journal: :Development 2003
Maria A Ros Randall D Dahn Marian Fernandez-Teran Kay Rashka Nicholas C Caruccio Sean M Hasso J James Bitgood Joseph J Lancman John F Fallon

We have analyzed a new limb mutant in the chicken that we name oligozeugodactyly (ozd). The limbs of this mutant have a longitudinal postaxial defect, lacking the posterior element in the zeugopod (ulna/fibula) and all digits except digit 1 in the leg. Classical recombination experiments show that the limb mesoderm is the defective tissue layer in ozd limb buds. Molecular analysis revealed that...

Journal: :iranian journal of microbiology 0
m j fatemi plastic & reconstructive surgery, department of plastic & reconstructive surgery and burn research center, hazrat fateme hospital, tehran university of medical sciences, tehran, iran. h bateni plastic & reconstructive surgeon, mehr private hospital, tehran, iran.

a chronic fungal infection in tropical regions, chromoblastomycosis is caused by dematiaceous fungi, the form-family of fungi imperfecti, usually affecting one lower limb at the site of a trauma but sometimes involving other areas of the body including head & neck. in this article, we report the case of a rare primary chromoblastomycosis of the palate and chest in a 27-year-old man who was succ...

   Background:The aim of this study is to find out the spatial and temporal expression of TGF-b1 during the tendon healing, after application of Platelet Rich Plasma (PRP). Methods: A patellar tendon defect model in rabbits was used for this purpose. 48 skeletally mature New Zealand White rabbits, weighing 3.5 kg, were used for this study. Equal numbers of animals from both groups were sacrific...

Journal: :Journal of Ayub Medical College, Abbottabad : JAMC 2007
Farmanullah Muhammad Shoaib Khan Syed Muhammad Awais

BACKGROUND Tibial bone defect lead to limb shortening and functional deficit and needs proper treatment. There are various treatment modalities for bone defect in long bone to restore length and function of the limb, i.e. bone grafting, vascularised bone graft, allograft and bone transport. Bone transport can be done through fixators (uniplaner or ring) and intramedullary nail system. This stud...

Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are bilateral and asymmetrical. They range from clinodactyly, absent or digitalised thumb, hypoplastic...

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