Brain morphometry driven by DTI data in Moebius Syndrome and Hereditary Congenital Facial Paresis

نویسندگان

  • Neda Sadeghi
  • Irini Manoli
  • Elizabeth Hutchinson
  • Carol Van Ryzin
  • Cibu Thomas
  • M. Okan Irfanoglu
  • Amritha Nayak
  • Chia-Ying Liu
  • Francis S. Collins
  • Ethylin Wang Jabs
  • Elizabeth C. Engle
  • Carlo Pierpaoli
چکیده

Section on Quantitative Imaging and Tissue Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA, Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA, Quantitative Medical Imaging Section, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD, USA, National Institute of Mental Health, Bethesda, MD, USA, Radiology and Imaging Sciences, National Institutes of Health, Bethesda, MD, USA,Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA, Departments of Neurology and Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, Howard Hughes Medical Institute, Chevy Chase, MD, United States

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منابع مشابه

Observations on the Pathology of the Moebius Syndrome.

The first report of the congenital facial diplegia syndrome, or Moebius syndrome, was that of Graefe (1880). Moebius reported cases in 1888 and 1892 and reviewed the prior case reports, thus gaining eponymic distinction. Since that time, some authors have broadened the definition of the Moebius syndrome, as for example, Henderson (1939), who considered some cases of congenital unilateral facial...

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Mirror Movements Identified in Patients with Moebius Syndrome

BACKGROUND Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial weakness in association with impairment in abduction of one or both eyes. Mirror movements are not known to be associated with Moebius syndrome. CASE REPORT We present three patients who meet minimum criteria for a diagnosis of Moebius syndrome and who also display mirror movements. DISCUSSION...

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An unusual case report showing overlapping Features of Poland and Moebius syndrome

[email protected] Phone no. +91 9501544877 Abstract Moebius and Poland syndromes are rare congenital anomalies. Poland syndrome (PS) is characterized by unilateral aplasia/hypoplasia of the breast and pectoralis muscle and ipsilateral deformities in the extremities. However, Moebius-Poland syndrome is rarer than the isolated syndromic conditions. Moebius syndrome is characterized by unilateral...

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Moebius syndrome

Moebius syndrome is a rare, nonprogressive neurological disorder (prevalence is estimated to be 0.002% of births) characterized by unilateral or bilateral facial paralysis and defective extraocular eye movements secondary to congenital paresis of the facial (VII) and abducens (VI) cranial nerves. These classic features of the syndrome are often accompanied by hypoglossal (XII), trigeminal (V), ...

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Moebius Syndrome: A Rare Case Report

Moebius syndrome is an extremely rare disorder. Only approximately few hundred cases have been reported in literature. In a nationwide survey reported in 2003, the prevalence of this syndrome was at least 0.002% of births for the years 1996 to 1998. The definition and diagnostic criteria for Moebius syndrome vary among authors. In most studies, it is defined as congenital facial weakness combin...

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تاریخ انتشار 2016