Results 101 to 110 of about 17,135 (242)

Outcomes of 87 small‐breed dogs surgically treated for Chiari‐like malformation and syringomyelia

Veterinary Surgery, EarlyView.
Abstract Objective To report the outcomes of titanium mesh (TM) cranioplasty without polymethylmethacrylate (PMMA), incorporating a deliberate gap between the foramen magnum decompression (FMD) surface and the TM, in small‐breed dogs with Chiari‐like malformation and syringomyelia (CM/SM). Study design Retrospective clinical study.
Sung Su Park, Ji Young Park, Ho Jae Han
wiley   +1 more source

Detección ecográfica y pronóstico de la ventriculomegalia fetal

Revista Chilena de Obstetricia y Ginecología, 2012
Antecedentes: La ventriculomegalia fetal es un signo ecográfico muy sensible para las alteraciones del sistema nervioso central fetal. La morbilidad asociada a la misma depende principalmente de la etiología y de la presencia de otras malformaciones ...
Mercedes Hernández S, Olivia Orribo M, Ingrid Martínez W, Ana I Padilla P, Margarita Álvarez de la Rosa R, Juan M Troyano L   +5 more
doaj  

Unique Presentation of Colpocephaly in a Preterm Triplet: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Colpocephaly is a rare congenital cerebral malformation characterised by disproportionate dilatation of the occipital horns of the lateral ventricles, most commonly associated with partial or complete agenesis of the corpus callosum.
Smita Dey, Vijayalakshmi Samudi
doaj   +1 more source

Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome [PDF]

, 2003
Primary ciliary dyskinesia (PCD), also referred to as immotile-cilia syndrome or Kartagener syndrome, is a group of genetic disorders caused by defective cilia leading to chronic sinupulmonary infection, situs inversus and reduced fertility.
Afzelius, Afzelius, Bloom, Bromley, Brueckner, Bryan, Chen, Daniel, De Santi, Dhein, Edwards, Greenstone, Guichard, Hackett, Ibañez-Tallon, Jabourian, Kelly, Losa, Mercier, Monnet, Nakamura, Nonaka, Olbrich, Pennarun, Picco, Pilu, Shimizu, Torikata, Vergani, Whitelaw   +29 more
core   +1 more source

An eye on long‐duration spaceflight: Controversies, countermeasures and challenges

Experimental Physiology, EarlyView.
Abstract Space flight‐associated neuroocular syndrome (SANS) is a consequence of long‐duration space flight and is detected in two‐thirds of astronauts. In‐flight, this can cause a change in the refraction of the eyes, requiring graded hypermetropic ‘superfocus adjustable’ glasses, optic nerve head oedema and choroidal folds.
Vincent Wing Sum Ng, Susan Patricia Mollan   +1 more
wiley   +1 more source

Three dimensional optical imaging of blood volume and oxygenation in the neonatal brain [PDF]

, 2006
Optical methods provide a means of monitoring cerebral oxygenation in newborn infants at risk of brain injury. A 32-channel optical imaging system has been developed with the aim of reconstructing three-dimensional images of regional blood volume and ...
Arridge, SR, Austin, T, Branco, G, Delpy, DT, Gibson, AP, Hebden, JC, Meek, JH, Wyatt, JS, Yusof, RM   +8 more
core   +1 more source

The outcome of fetal ventriculomegaly

The British Journal of Radiology, 1994
Abstract Over a 5 year period 38 cases of fetal ventriculomegaly were diagnosed at Queen's Medical Centre, Nottingham. There were 12 cases of spina bifida and all patients opted for a termination of pregnancy. There were 15 cases of isolated ventriculomegaly comprising seven cases of aqueduct stenosis, four abnormalities of the corpus ...
P, Twining, T, Jaspan, J, Zuccollo
openaire   +2 more sources

Clinical Insights From a Case of Sifrim‐Hitz‐Weiss Syndrome With a CHD4 Variant: Expanding the Phenotypic Spectrum and Its Response to Growth Hormone Therapy

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1403-1410, June 2026.
ABSTRACT To enhance clinicians' understanding of Sifrim‐Hitz‐Weiss syndrome (SIHIWES), this study investigated the clinical phenotypes, genetic characteristics, and response to growth hormone therapy in a patient. A case of a patient with global developmental delay and distinctive facial features is presented.
Jianmei Zhang, Shuangzhong Chen, Guanping Dong, Suhong Yang, Ping Wang, Qiong Zhou, Pingping Wang   +6 more
wiley   +1 more source

Homozygous Achondroplasia With Long‐Term Survival: Growth Patterns, Medical Interventions, and Practice Implications

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1372-1377, June 2026.
ABSTRACT Homozygous achondroplasia is widely considered perinatal lethal by the medical community. In this case series, we report two children from a single family with longer‐term survival. One child lived for 17 months and the other was 60 months at the time of publication.
Hannah Singerline, Jason Laufman, Kimberly Wallis, Michelle Merrill   +3 more
wiley   +1 more source

Hydrocephalus in Patients With Diffuse Intrinsic Pontine Glioma: A Systematic Review of the Literature

Pediatric Blood &Cancer, Volume 73, Issue 5, May 2026.
ABSTRACT Hydrocephalus is an underexplored complication in patients with diffuse intrinsic pontine glioma (DIPG). This systematic review aims to evaluate the incidence, diagnosis, management strategies, and clinical impact of hydrocephalus in DIPG.
Olga Nigro, Biassoni Veronica, Schiavello Elisabetta, Giussani Carlo Giorgio, Schiariti Marco, Pluderi Mauro, Massimino Maura   +6 more
wiley   +1 more source