نتایج جستجو برای: caudal dysplasia sequence

تعداد نتایج: 445664  

Journal: :acta medica iranica 0
davari tanha f googol n kaveh m

caudal regression syndrome (caudal dysplasia sequence) is a rare congenital malformation. it has a spectrum ranging from simple anal atresia to the absence of sacral, lumbar and possibly lower thoracic vertebrae and the most severe form called sirenomelia (mermaid syndrome). sirenomelia has a sole characteristic, which is the limbs fusion, with multiple internal structural abnormalities particu...

Journal: :The Journal of the Association of Physicians of India 2003
S Basu N Nair

Caudal dysplasia sequence (CDS) comprises developmental anomalies of the caudal vertebrae, neural tube, urogenital and digestive organs, and hind limbs, the precursors of all of which are derived from the caudal eminence. Although the syndrome is well recognized, the etiology and pathogenetic mechanisms are poorly understood. We report syringomyelia in association with the CDS, which has not be...

جباری, محمود, عماد ممتاز, حسین,

Introduction: Jarcho- Levin syndrome and caudal regression syndrome are rare syndromes with clinical and radiologic findings of cervical and thoracic vertebral anomalies with rib deformities (jarcho-levin syndrome) and sacrococcygeal agenesis, lower extremity anomalies, truncated spinal cord and neurogenic bladder (caudal regression syndrome). There are only one report of simultaneous existen...

Journal: :British Journal of Surgery 2021

Abstract Background A metaplasia-dysplasia–carcinoma sequence is the most plausible carcinogenic pathway for gallbladder cancer. Although incidence of carcinoma increasing, little known about its precancerous lesions. The aim this study was to determine temporal changes in prevalence low-grade dysplasia (LGD), high-grade (HGD) and adenocarcinoma associated risk factors. Methods We retrospective...

Journal: :Nature Reviews Gastroenterology & Hepatology 2011

Journal: :Human molecular genetics 2005
Catherine E Keegan Janna E Hutz Tobias Else Maja Adamska Sonalee P Shah Amy E Kent John M Howes Wesley G Beamer Gary D Hammer

Adrenocortical dysplasia (acd) is a spontaneous autosomal recessive mouse mutant with developmental defects in organs derived from the urogenital ridge. In surviving adult mutants, adrenocortical dysplasia and hypofunction are predominant features. Adults are infertile due to lack of mature germ cells, and 50% develop hydronephrosis due to ureteral hyperplasia. We report the identification of a...

Journal: :Developmental dynamics : an official publication of the American Association of Anatomists 2011
Randal X Moldrich Cecilia Mezzera William M Holmes Sailaja Goda Sam J Brookfield Alastair J Rankin Emily Barr Nyoman Kurniawan Deborah Dewar Linda J Richards Guillermina López-Bendito Tomoko Iwata

The fibroblast growth factor receptor 3 (Fgfr3) is expressed in a rostral(low) to caudal(high) gradient in the developing cerebral cortex. Therefore, we hypothesized that Fgfr3 contributes to the correct morphology and connectivity of the caudal cortex. Overall, the forebrain structures appeared normal in Fgfr3(-/-) mice. However, cortical and hippocampal volumes were reduced by 26.7% and 16.3%...

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