نتایج جستجو برای: anterior fontanelle

تعداد نتایج: 124764  

Journal: :Pediatrics and neonatology 2016
Atanu Kumar Dutta Sumita Danda

http://dx.doi.org/10.1016/j.pedneo.2015.09.005 1875-9572/Copyright a 2015, Taiwan Pediatric Association. Published CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd third degree consanguineous parentage and delivered at 33 weeks of gestation by caesarean section. The weight at birth was 1.02 kg, and the occipitofrontal circumference was 30.5 cm. She had a wide anterior fontanell...

Journal: :بینا 0
محمد پاکرولن m pakravan ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم فریده شریفی پور f sharifipoor jondi shapoor university of medical sciences, ahvaz, iranدانشگاه علوم پزشکی اهواز شاهین یزدانی sh yazdani ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم نسیم کوهستانی n kohestani ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم نسیم عموهاشمی n amohashemi ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم مهدی یاسری m yaseri دانشکده بهداشت- دانشگاه علوم پزشکی تهران

purpose: to compare anterior segment and ocular biometric parameters of unaffected fellow eyes of patients with a previous attack of acute angle closure (aac), primary angle closure suspect (pacs) eyes, and normal eyes; and to assess the risk of developing aac in pacs. methods: in this prospective comparative observational case series, 16 unaffected fellow eyes of patients with a previous attac...

2014
Sherien A. Shohoud Waleed A. Azab Tarek M. Alsheikh Rania M. Hegazy

BACKGROUND We report a case of a neonate with proximal spinal muscular atrophy (SMA) type 1 (also known as Werdnig-Hoffmann disease or severe infantile acute SMA) associated with a Blake's pouch cyst; a malformation that is currently classified within the spectrum of Dandy-Walker complex. The association of the two conditions has not been previously reported in the English literature. A compreh...

2013
Benvon C. Cramer Sigrid Jequier Augustin M. O'Gorman

To determine the value of ultrasound scanning of the craniocervical junction in neonates via a posterior approach, we examined 50 infants with normal posterior fossae, 10 with congenital abnormalities, and eight with intracranial hemorrhage. Good evaluation of the cisterna magna, medulla, tonsils, vermis, cervical cord, and central canal was possible in most cases. In nine patients with spinal ...

Journal: :Indian pediatrics 2004
D P Muzumdar A Goel

agents of acute diarrhea in the first 3 years of life: Hospital-based study. Bacterial, viral and parasitic enteric pathogens associated with acute diarrhea in hospitalized children from northern Jordan. A 10-month-old female infant, born of nonconsanguineous parents, full-term normal delivery presented with a large swelling over the occipital region since birth. The child could not hold the he...

Journal: :Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine 2001
A Visentin G Pilu P Falco L Bovicelli

The objective of this study was to assess the feasibility of using the frontal suture as an acoustic window to visualize sonographically the midline cerebral structures (transfrontal view) in midtrimester fetuses. The study design was prospective and observational. In 124 healthy fetuses and in 2 fetuses with agenesis of the corpus callosum at 19 to 24 weeks' gestation, an attempt was made to o...

Journal: :Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2005
C Faro B Benoit P Wegrzyn R Chaoui K H Nicolaides

OBJECTIVE To describe the morphology of the frontal bones and metopic suture at 9-34 weeks of gestation using three-dimensional (3D) ultrasonography. METHODS This was a cross-sectional study of the frontal bones and metopic suture in 16 fetuses at 9-34 weeks of gestation. 3D ultrasonography was used to obtain volumes of the whole fetal skull in the mid-sagittal plane. The volumes were analyze...

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1974

Journal: :Human molecular genetics 2014
Frank J Kaiser Morad Ansari Diana Braunholz María Concepción Gil-Rodríguez Christophe Decroos Jonathan J Wilde Christopher T Fincher Maninder Kaur Masashige Bando David J Amor Paldeep S Atwal Melanie Bahlo Christine M Bowman Jacquelyn J Bradley Han G Brunner Dinah Clark Miguel Del Campo Nataliya Di Donato Peter Diakumis Holly Dubbs David A Dyment Juliane Eckhold Sarah Ernst Jose C Ferreira Lauren J Francey Ulrike Gehlken Encarna Guillén-Navarro Yolanda Gyftodimou Bryan D Hall Raoul Hennekam Louanne Hudgins Melanie Hullings Jennifer M Hunter Helger Yntema A Micheil Innes Antonie D Kline Zita Krumina Hane Lee Kathleen Leppig Sally Ann Lynch Mark B Mallozzi Linda Mannini Shane McKee Sarju G Mehta Ieva Micule Shehla Mohammed Ellen Moran Geert R Mortier Joe-Ann S Moser Sarah E Noon Naohito Nozaki Luis Nunes John G Pappas Lynette S Penney Antonio Pérez-Aytés Michael B Petersen Beatriz Puisac Nicole Revencu Elizabeth Roeder Sulagna Saitta Angela E Scheuerle Karen L Schindeler Victoria M Siu Zornitza Stark Samuel P Strom Heidi Thiese Inga Vater Patrick Willems Kathleen Williamson Louise C Wilson Hakon Hakonarson Fabiola Quintero-Rivera Jolanta Wierzba Antonio Musio Gabriele Gillessen-Kaesbach Feliciano J Ramos Laird G Jackson Katsuhiko Shirahige Juan Pié David W Christianson Ian D Krantz David R Fitzpatrick Matthew A Deardorff

Cornelia de Lange syndrome (CdLS) is a multisystem genetic disorder with distinct facies, growth failure, intellectual disability, distal limb anomalies, gastrointestinal and neurological disease. Mutations in NIPBL, encoding a cohesin regulatory protein, account for >80% of cases with typical facies. Mutations in the core cohesin complex proteins, encoded by the SMC1A, SMC3 and RAD21 genes, to...

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