نتایج جستجو برای: spondylothoracic dysplasia

تعداد نتایج: 28629  

2006
R D Odze

This review focuses on the pathological features of dysplasia in Barrett’s oesophagus. Two categorisation schemes are used for grading dysplasia in the gastrointestinal tract, including Barrett’s oesophagus. The inflammatory bowel disease dysplasia morphology study group system is the one most commonly used in the USA. However, some European and most far Eastern countries use the Vienna classif...

Journal: :Journal of clinical pathology 2006
R D Odze

This review focuses on the pathological features of dysplasia in Barrett's oesophagus. Two categorisation schemes are used for grading dysplasia in the gastrointestinal tract, including Barrett's oesophagus. The inflammatory bowel disease dysplasia morphology study group system is the one most commonly used in the USA. However, some European and most far Eastern countries use the Vienna classif...

Journal: :international journal of pediatrics 0
majid mahallei assistant professor of pediatrics and neonatology, tabriz university of medical sciences, tabriz, iran. manizheh mostafa gharehbaghi professor of pediatrics and neonatology, women’s reproductive health research center, tabriz university of medical sciences, tabriz, iran. leila majidzadeh pediatrician, tabriz university of medical sciences, tabriz, iran. nazanin hazhir general practitioner, tabriz university of medical sciences, tabriz, iran.

background bronchopulmonary dysplasia (bpd) is one of the most common serious squeal of preterm infants. it involves approximately one quarter of infants with birth weight less than 1500 grams and 30% of less than 1000 grams. vitamin a has been shown to reduce bpd rate. we compared efficacy of low and high doses of vitamin a for prevention of bpd in very low birth weight preterm infants. materi...

Journal: :international journal of pediatrics 0
moein mobini department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. rahim vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. saba vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran.

mccune-albright syndrome (mas) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. the disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities.  we describe a girl patient with mas having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. clinical presentat...

Journal: :iranian journal of medical sciences 0
suzanne tanya nethan department of oral medicine and radiology, saraswati dental college, lucknow, uttar pradesh, india shruti sinha department of oral medicine and radiology, saraswati dental college, lucknow, uttar pradesh, india sunira chandra department of oral medicine and radiology, saraswati dental college, lucknow, uttar pradesh, india

the ellis-van creveld (evc) syndrome is a chondroectodermal dysplasia and is characterized by the cardinal features of disproportionate short stature, polydactyly, hidrotic ectodermal dysplasia, and congenital heart malformations, along with other skeletal and dental abnormalities. it is a rare condition, with very few cases reported in the medical literature. it is inherited as an autosomal re...

Journal: :hepatitis monthly 0
babak behnam cellular and molecular research center, iran university of medical sciences, tehran, ir iran; department of medical genetics and molecular biology, faculty of medicine, iran university of medical sciences, tehran, ir iran; ali-asghar children hospital, iran university of medical sciences, tehran, ir iran marjan shakiba department of pediatrics, mofid hospital, shahid beheshti university of medical sciences, tehran, ir iran ali ahani department of genetics and reproduction, avicenna research center, tehran, ir iran maryam razzaghy azar ali-asghar children hospital, iran university of medical sciences, tehran, ir iran; endocrine and metabolic research center, tehran university of medical sciences, tehran, ir iran; endocrine and metabolic research center, diabetes and metabolic clinic, shahrivar alley, north kargar ave. 1411715851, tehran, ir iran. tel: +98-2166942903, fax: +98-2166421054,

early-onset diabetes, liver dysfunction, growth retardation, spondyloepiphyseal dysplasia, and tendency to skeletal fractures due to osteopenia are characteristics of wolcott-rallison syndrome (wrs). eukaryotic translation initiation factor 2α kinase (eif2ak3) is the only known gene, which is responsible for this rare autosomal recessive disorder. here, we report two siblings a girl and a boy w...

Journal: :iranian journal of child neurology 0
marjan shakiba assistant professor of pediatric pediatric endocrinology, mofid children hospital, shahid beheshti university of medical sciences, tehran, iran habibe nezhad bieglari pediatrician mohammad reza alaee associate professor of pediatric endocrinology, mofid children hospital, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: shakiba m, nejad biglari h, alaee mr. digital and dental malformation and short stature in a patient with neurological problems: a variant of the oculodentodigital dysplasia syndrome or a new syndrome?iran j child neurol autumn 2012; 6(4): 51-54.   abstract several syndromes have been recognized with digital abnormality and cns involvement such as oculodentodigital dys...

Journal: :iranian journal of immunology 0
mete eyigor akdeniz university medical faculty, department of medical microbiology hulya eyigor department of ent head and neck surgery, antalya education and research hospital ustun osma department of ent head and neck surgery, antalya education and research hospital mustafadeniz yilmaz department of ent head and neck surgery, antalya education and research hospital nuray erin akdeniz university medical faculty, department of medical pharmacology omer tarik selcuk department of ent head and neck surgery, antalya education and research hospital cem sezer

background: although the imbalance of cytokines in head and neck squamous cell carcinoma (hnscc) is well known, there is scarce data regarding its occurrence during dysplasia, before the malignant transformation. objective: to determine whether laryngeal dysplasia patients show a different cytokine profile than patients with cancer and healthy controls. methods: seventeen newly diagnosed, untre...

2011
Syoji Kobashi Nobuyoshi Kawakami Yuri T. Kitamura Kuriko K. Shimono Kei Kuramoto Masako Taniike Tomomoto Ishikawa Yutaka Hata

About 80% of paediatric intractable epilepsy patients have accompanying cortical dysplasia. However, there are no established methods for noninvasive detection of cortical dysplasia. This paper proposes a novel method for automatically detecting cortical dysplasia using paediatric MR images. In order to evaluate cortical dysplasia in MR images, texture features and fractal dimension were extrac...

2017
Weihao Li Yanhua Xu Song Li

Ectodermal dysplasia, which affects ectodemal derivatives, currently is an X-linked recessive inheritary hypohydrotic ectodermal dysplasia. Patients with ectodermal dysplasia usually characterized by congenital teeth loss, abnormal teeth and inherited through female carriers. In this case report, we present a 5 years old boy of China ethnicity with mandibular anodontia, a rare dental dysplasia ...

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