Results 111 to 120 of about 1,067 (162)
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Moebius Syndrome in Kallmann Syndrome
Archives of Neurology, 1975A girl born with congenital paresis of cranial nerves III, IV, and VII (Moeblus syndrome) subsequently developed a progressive peripheral neuropathy. There was suggestive evidence of a familial neuropathy with autosomal dominant inheritance in three family members. The patient also had hypogonadotrophic hypogonadism and anosmia (Kallmann syndrome).
A E, Rubinstein +3 more
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Bellʼs Palsy in Moebius Syndrome
Ophthalmic Plastic & Reconstructive Surgery, 1991We report a case of unilateral transient and reversible facial paresis, which was superimposed on a congenital bifacial palsy in a young adult with Moebius syndrome. Our case illustrates the potential for two conditions, both affecting the facial nerve and both of unknown etiology, to be juxtaposed in a single individual.
D L, Budenz +3 more
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Moebius syndrome with oral involvement
International Journal of Paediatric Dentistry, 2002Summary. The oral findings of 12 patients with Moebius syndrome are described. Facial weakness, hypoplastic upper lip, microstomia, mouth‐angle drooping, hypoplasia of mandible, gothic palate, tongue weakness, fissured tongue, tongue atrophy and open bite were found.
M V X, De Serpa Pinto +2 more
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Autistic Behaviour in Moebius Syndrome
Acta Paediatrica, 1989ABSTRACT. Seventeen children and young adults with Moebius syndrome were examined with a view to finding symptoms of autism. Some 40% of the group showed all or many of the symptoms typical of autistic disorder. The high frequency of autistic symptoms in Moebius syndrome might be a marked overrepresentation and could be suggestive of a common ...
C, Gillberg, S, Steffenburg
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Neuropathological findings in Moebius syndrome
Clinical Genetics, 1998Pathological findings in two patients with Moebius syndrome and lethal fetal akinesia sequence are described. In both patients a congenital brain stem malformation with neuronal loss in the cranial nerve nuclei and tegmental microcalcifications was observed.
M, Lammens +6 more
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INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH
Moebius syndrome is a disease that is characterized by congenital unilateral or bilateral non-progressive palsy of facial and abducens nerves i.e cranial nerves VI and VII. It leads to unilateral or bilateral weakness of the face along with limited abduction of the eyes. Facial weakness generally includes the inability to smile, chew or close the mouth,
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Moebius syndrome is a disease that is characterized by congenital unilateral or bilateral non-progressive palsy of facial and abducens nerves i.e cranial nerves VI and VII. It leads to unilateral or bilateral weakness of the face along with limited abduction of the eyes. Facial weakness generally includes the inability to smile, chew or close the mouth,
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Neurology, 1970
SUMMARYA patient has been described with Moebius syndrome in whom there was clinical paralysis of the muscles supplied by the third, fourth, sixth, and seventh cranial nerves. Limb muscle biopsy studies and electromyography of the limb muscle suggest denervation of an “anterior horn cell” type of abnormality in the spinal cord.
W H, Olson +3 more
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SUMMARYA patient has been described with Moebius syndrome in whom there was clinical paralysis of the muscles supplied by the third, fourth, sixth, and seventh cranial nerves. Limb muscle biopsy studies and electromyography of the limb muscle suggest denervation of an “anterior horn cell” type of abnormality in the spinal cord.
W H, Olson +3 more
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Facial animation in patients with Moebius and Moebius-like syndromes
International Journal of Oral and Maxillofacial Surgery, 2010Moebius syndrome, a rare congenital disorder of varying severity, involves multiple cranial nerves and is characterised predominantly by bilateral or unilateral paralysis of the facial and abducens nerves. Facial paralysis causes inability to smile and bilabial incompetence with speech difficulties, oral incompetence, problems with eating and drinking,
FERRARI, Silvano +4 more
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Facial animation in children with Moebius and Moebius-like syndromes
Journal of Pediatric Surgery, 2009Moebius syndrome, a rare congenital disorder of varying severity, involves multiple cranial nerves and is characterized predominantly by bilateral or unilateral paralysis of the facial and abducens nerves. The paralysis of the VI and VII cranial nerves leads to a lack of function in the muscles they supply.
Bianchi B. +4 more
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Journal of oral surgery (American Dental Association : 1965), 1975
A case report of Moebius syndrome is presented. The syndrome includes bilateral facial and abducens nerve paresis, muscular hypoplasia, adactylia, club foot, and possible mental retardation. This particular patient had bilateral facial and abducens nerve paralysis, mandibular hypoplasia, pectoral muscle hypoplasia, adactylia, and bilateral clubbed ...
R, Federman, J C, Stoopack
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A case report of Moebius syndrome is presented. The syndrome includes bilateral facial and abducens nerve paresis, muscular hypoplasia, adactylia, club foot, and possible mental retardation. This particular patient had bilateral facial and abducens nerve paralysis, mandibular hypoplasia, pectoral muscle hypoplasia, adactylia, and bilateral clubbed ...
R, Federman, J C, Stoopack
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