نتایج جستجو برای: macrocephaly

تعداد نتایج: 695  

Journal: :Journal of the Belgian Society of Radiology 2013

Journal: :Journal of medical genetics 2011
Robert Pilarski Julie A Stephens Ryan Noss James L Fisher Thomas W Prior

BACKGROUND Cowden syndrome (CS) is associated with benign hamartomatous lesions and risks for thyroid, breast and endometrial cancers. Bannayan-Riley-Ruvalcaba syndrome is an allelic disorder characterised by macrocephaly, intestinal polyps, lipomas, and pigmented penile macules. Diagnostic criteria for CS are based on the presence of a range of clinical features. However, prior data on the com...

Journal: :AJNR. American journal of neuroradiology 2003
Erin D Bigler David F Tate E Shannon Neeley Lara J Wolfson Michael J Miller Sara A Rice Howard Cleavinger Carol Anderson Hilary Coon Sally Ozonoff Michael Johnson Elena Dinh Jeff Lu William Mc Mahon Janet E Lainhart

BACKGROUND AND PURPOSE Because of increased prevalence of macrocephaly in autism, head size must be controlled for in studies that examine volumetric findings of the temporal lobe in autistic subjects. We prospectively examined temporal lobe structures in individuals with autism who were normocephalic or macrocephalic (head circumference > 97th percentile) and in control subjects who were normo...

Journal: :Asploro Journal of Biomedical and clinical Case Reports 2022

A 19-year-old man with a BMI of 23.8 kg/m2 (5 ft 7 in; 152 lbs) presented the concern 3 years progressively enlarging head leading to an increase in hat size. The patient fulfilled criteria for macrocephaly as his circumference was 62 cm, which above 97th percentile age [1]. CT revealed homogeneous bilateral hypertrophy temporalis, masseter, and medial pterygoid muscles no evidence neoplastic p...

2015
David Miller Patrick Barnes Marvin Miller

Infants with the triad (neurologic dysfunction, subdural hematoma [SDH], and retinal hemorrhage) are often diagnosed as victims of shaken baby syndrome. Medical conditions/predisposing factors to developing the triad are often dismissed: short falls, birth-related SDH that enlarges, macrocephaly, sinus/cortical vein thrombosis, and others. Six infants with the triad are described in which child...

2018
Cathryn Poulton Gareth Baynam Clarissa Yates Hamid Alinejad-Rokny Simon Williams Helen Wright Karen J Woodward Soruba Sivamoorthy Joanne Peverall Peter Shipman David Ravine John Beilby Julian Ik-Tsen Heng

BACKGROUND Pallister-Killian syndrome (PKS) is a rare multisystem developmental syndrome usually caused by mosaic tetrasomy of chromosome 12p that is known to be associated with neurological defects. METHODS We describe two patients with PKS, one of whom has bilateral perisylvian polymicrogyria (PMG), the other with macrocephaly, enlarged lateral ventricles and hypogenesis of the corpus callo...

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