نتایج جستجو برای: facial anomaly
تعداد نتایج: 98946 فیلتر نتایج به سال:
A newborn male with Möbius syndrome, Poland anomaly, and dextrocardia is described. This is the second case reported of Poland-Möbius syndrome associated with dextrocardia. The patient presented with strabismus, facial diplegia, difficulty in swallowing, hypoplasia of the left pectoralis major muscle, partial absence of the upper costal cartilages, absence of the left areola, hypoplasia of the ...
We are reporting here, a case of the Lenz syndrome in a neonate who was brought to the Paediatric OPD, Kasturba Medical College Hospital, Attavar, Mangalore India, with the complaints of poor suckling since birth and abnormal facial features. Altogether, the characteristic congenital abnormal findings in Lenz syndrome, which comprise of microophthalmia, ear anomalies, microcephaly, skeletal and...
The conotruncal anomaly face syndrome was described in a Japanese publication in 1976 and comprises dysmorphic facial appearance and outflow tract defects of the heart. The authors subsequently noted similarities to Shprintzen syndrome and DiGeorge syndrome. Chromosome analysis in five cases did not show a deletion at high resolution, but fluorescent in situ hybridisation using probe DO832 show...
Digeorge syndrome is caused by microdeletion of a large region of chromosome 22q11.2 lead to the abnormal development of the third and fourth pharyngeal pouches. This syndrome is characterized by hypoparathyroidism, cellular immune deficiency secondary to thymic hypoplasia, congenital heart disease and dysmorphic facial features. In this case report, we describe a 4month old boy who presented w...
how to cite this article: inaloo s, katibeh p. guillain-barre syndrome presenting with bilateral facial nerve palsy. iran j child neurol. 2014 winter;8(1):69-71. objective this case study is about an 11-year-old girl with bilateral facial weakness, abnormal taste sensation, and deep tendon reflexes of both knees and ankles were absent. however, the muscle power of the lower and upper extremiti...
INTRODUCTION Peters anomaly is a rare developmental malformation involving the anterior segment of the eye, which culminates in amblyopia or congenital blindness. Multiple ocular and/or systemic malformations have been observed with this anomaly, and novel comorbidities continue to be reported. CASE PRESENTATION The probands were monozygotic twin boys (twin I and twin II) born to consanguineo...
Background and Objective: Congenital craniofacial anomalies emerge as changes in structure, function and metabolism at birth. This study aimed to identify congenital malformations of the face and different non-healed and healed craniofacial fractures and their epidemiology in people younger than 18 years in the province of Zanjan. Materials and Methods: This study was carried out on all urba...
Objectives. Asymmetric facial appearance may originate from abnormalities of facial musculature or facial innervation. We describe clinical features of congenital hypoplasia of depressor anguli oris muscle in a child. Material and Methods. Chart of a 10-month-old female referred to a tertiary care pediatric hospital for assessment of facial paralysis was reviewed. Data included relevant history...
Through respectively adding September DE3 tide and March DE3 tide at the low boundary of Global Coupled Ionosphere-Thermosphere-Electrodynamics Model, Institute of Geology and Geophysics, Chinese Academy of Sciences (GCITEM-IGGCAS), we simulate the influence of DE3 tide on the equinoctial asymmetry of the zonal mean ionospheric electron density. The influence of DE3 tide on the equinoctial asym...
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