نتایج جستجو برای: cns developmental anomalies

تعداد نتایج: 266989  

انصار, اکرم, فرشچیان, محمود, فریدون نژاد, مرتضی,

Introduction: Nevoid BCC syndrome (Gorline syndrome) is a familial disorder with autosomal dominant inheritense. This syndrome is combination of multiple BCC that occurs at an early age, characteristic faces with: frontal bossing, broad nasal bridge and hypertelorism, jaw cysts, palmoplanter pitting, macrocephaly, skeletal and spinal anomalies include bifid ribes, cervical rib and kyphoscoliosi...

AH Ehsani F Farahani N Ghandi Sh Yazdanian

Becker's naevus is an acquired persistent asymmetrical area of skin pigmentation, sometimes showing evidence of increased androgen sensitivity, and colocalizing with other developmental anomalies. We report a 30-year-old woman with clinical findings compatible with Becker's naevus on her right breast accompanied with hypoplasia of ipsilateral breast.

Journal: :Case Reports in Clinical Medicine 2023

Intraventricular haemorrhage (IVH) is an extremely rare and poorly described complication of central nervous system Tuberculosis (CNS-TB). In this study, we report the case a 42-year-old man who presented with weakness left hemibody diffuse headache, altered consciousness associated fever. No notion contagion was noted. Brain computed tomography (CT) showed hematoma in occipital horns lateral v...

2013
Alessia Indrieri Ivan Conte Giancarlo Chesi Alessia Romano Jade Quartararo Rosarita Tatè Daniele Ghezzi Massimo Zeviani Paola Goffrini Ileana Ferrero Paola Bovolenta Brunella Franco

Mitochondrial-dependent (intrinsic) programmed cell death (PCD) is an essential homoeostatic mechanism that selects bioenergetically proficient cells suitable for tissue/organ development. However, the link between mitochondrial dysfunction, intrinsic apoptosis and developmental anomalies has not been demonstrated to date. Now we provide the evidence that non-canonical mitochondrial dependent a...

درخشان, جهانگیر,

Developmental defect of Mullerian duct is a congenital malformation characterized by anomalies in famale upper genital organs. As the anomaly is associated with obstruction of the duct, other congenital anomalies of urinary tract specially ipsilateral ranal agenesis are common. This anomaly is often discovered in adolescent period and is usually asymptomatic until puberty. To discover this anom...

Journal: :The British journal of ophthalmology 1965
H E Henkes

RIEGER'S dysgenesis mesodermalis iridis et corneae, caused by a faulty differentiation in the anterior segment, is not limited to the mesodermal structures of the eye, but demonstrates a range of ectodermal anomalies as well. This is why Hagedoorn (1937) suggested the term "dysgenesis mesostromalis", stressing the frequent occurrence of ectodermal developmental anomalies of the iris and lens, c...

Journal: :Open Access Journal of Dental Sciences 2019

2015
Dianne Gerrelli Steven Lisgo Andrew J. Copp Susan Lindsay

Congenital anomalies are a significant burden on human health. Understanding the developmental origins of such anomalies is key to developing potential therapies. The Human Developmental Biology Resource (HDBR), based in London and Newcastle, UK, was established to provide embryonic and fetal material for a variety of human studies ranging from single gene expression analysis to largescale geno...

Journal: :Health information management : journal of the Health Information Management Association of Australia 2004
Khin Than Win Hai Phung Lis Young Mai Tran Carole Alcock Ken Hillman

This article discusses the risk assessment of a health information system. A case study was conducted at the South Western Sydney Area Health Service to examine the potential risks of the Maternal and Infant Network (MINET) health information system using Failure Mode Effect Analysis (FMEA). FMEA was conducted by utilising safety attributes identified by the authors. Potential failure modes of ...

Müllerian anomalies are very common, and a frequent cause of infertility. The most used classification system until now, proposed by the American Society for Reproductive Medicine in 1988, categorizes comprehensively uterine anomalies but fails to classify defects of the cervix or vagina. This is based on a developmental theory that postulates that müllerian duct fusion is unidirectional, begin...

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