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TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, ISSN 1306-0015, 03/2012, Volume 47, Issue 1, pp. 64 - 66
Facial palsy is a sporadic disease related to cold exposure, infections and psychogenic factors. In this case report, we present a 14 years old boy with... 
facial palsy | familial | PARALYSIS | BELLS-PALSY | PEDIATRICS | Bell's palsy
Journal Article
Turk Pediatri Arsivi, ISSN 1306-0015, 2012, Volume 47, Issue 1, pp. 67 - 69
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2013, Volume 49, Issue 4, pp. 289 - 291
Journal Article
Book
Turkish Pediatrics Archive, ISSN 1306-0015, 03/2012, p. 64
Yuz felci soguga maruz kalma, enfeksiyon ve psikojenik nedenlerle iliskilendirilmis nadir bir durumdur. Burada yuz felciyle basvuran 14 yasindaki erkek hasta... 
Care and treatment | Paralysis, Facial | Familial diseases | Diagnosis | Children | Diseases
Journal Article
Annals of Physical and Rehabilitation Medicine, ISSN 1877-0657, 07/2018, Volume 61, pp. e262 - e262
Journal Article
European Archives of Oto-Rhino-Laryngology, ISSN 0937-4477, 04/2000, Volume 257, Issue 3, pp. 117 - 119
The etiology of idiopathic facial palsy (IFP) is still not defined. Familial inheritance has been found in 4–14% of cases. Among 116 patients with IFP admitted... 
Familial idiopathic facial palsy | Human leukocyte antigen | familial idiopathic facial palsy | human leukocyte antigen | BELLS-PALSY | OTORHINOLARYNGOLOGY | Facial Paralysis - genetics | Follow-Up Studies | Pedigree | Gene Frequency | Humans | Adult | Female | Male | Histocompatibility Antigens Class I - genetics | Index Medicus
Journal Article
Pediatric Neurology Briefs, ISSN 1043-3155, 06/2004, Volume 18, Issue 6, pp. 42 - 42
Three males with congenital facial palsy from 3 generations in the same family are reported from the Floating Hospital for Children, Tufts-New England Medical... 
Etiology | Familial Congenital Facial Palsy | Tympanic Portion
Journal Article
Neurology India, ISSN 0028-3886, 12/2009, Volume 57, Issue 6, pp. 783 - 784
Journal Article
Muscle and Nerve, ISSN 0148-639X, 05/2010, Volume 41, Issue 5, pp. 679 - 684
Hereditary amyloidosis of the Finnish type (HAF, or familial amyloid polyneuropathy type IV) is an autosomal dominant disease that has been described most... 
Corneal lattice dystrophy | Familial amyloid neuropathy | Gelsolin | Facial palsy | Hereditary amyloidosis | facial palsy | SUBSTITUTION | POLYNEUROPATHY | LIVER-TRANSPLANTATION | GELSOLIN AMYLOIDOSIS | gelsolin | familial amyloid neuropathy | corneal lattice dystrophy | FAF | NEUROSCIENCES | CLINICAL NEUROLOGY | GENE | MUTATION | hereditary amyloidosis | EXPERIENCE | Peripheral Nervous System Diseases - diagnosis | Genetic Testing | Cranial Nerve Diseases - genetics | Humans | Middle Aged | Facial Nerve Diseases - metabolism | Male | Peripheral Nervous System Diseases - physiopathology | Amyloid Neuropathies, Familial - physiopathology | Young Adult | Electrodiagnosis | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | DNA Mutational Analysis | Inheritance Patterns - genetics | Adult | Female | Peripheral Nerves - metabolism | Peripheral Nervous System Diseases - genetics | Cranial Nerve Diseases - physiopathology | Disability Evaluation | Amyloid Neuropathies, Familial - genetics | Cranial Nerves - metabolism | Genotype | Oculomotor Nerve Diseases - diagnosis | Corneal Dystrophies, Hereditary - diagnosis | Facial Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - metabolism | Hypoglossal Nerve Diseases - metabolism | Mutation - genetics | Oculomotor Nerve Diseases - physiopathology | Cranial Nerve Diseases - diagnosis | Peripheral Nerves - physiopathology | Neurologic Examination | Genetic Markers - genetics | Adolescent | Finland | Cranial Nerves - physiopathology | Aged | Gelsolin - genetics | Germany | Oculomotor Nerve Diseases - metabolism | Amyloid Neuropathies, Familial - diagnosis | Index Medicus
Journal Article
Strabismus, ISSN 0927-3972, 2001, Volume 9, Issue 3, pp. 137 - 141
Introduction Idiopathic facial nerve palsy is a common neurologic condition but episodes of ophthalmoplegia in these patients are uncommon. Materials and... 
Ophthalmoplegia | Familial cranial nerve palsy | Bell's palsy | Facial nerve palsy | Recurrence | Humans | Middle Aged | Male | Bell Palsy - complications | Bell Palsy - genetics | Aged, 80 and over | Adult | Female | Remission, Spontaneous | Aged | Ophthalmoplegia - complications | Ophthalmoplegia - genetics | Retrospective Studies | Index Medicus
Journal Article
Acta Otorrinolaringologica Espanola, ISSN 0001-6519, 1997, Volume 48, Issue 5, pp. 405 - 408
Journal Article
by Amit, R and Amit, R
European Journal of Pediatrics, ISSN 0340-6199, 1987, Volume 146, Issue 6, pp. 608 - 609
Familial Bell's palsy is uncommon and its genetic pattern is not well established. In this report, four female members of one family, the patient, her mother,... 
Facial palsy | Familial | Facial Paralysis - genetics | Disease Susceptibility | Humans | Adolescent | Sex Factors | Aging | Female | Facial Paralysis - drug therapy | Prednisone - therapeutic use | Index Medicus
Journal Article
12/2009
Bell′s palsy is a peripheral facial palsy of sudden onset. The etiology of Bell′s palsy is unknown and hereditary components may play a role in familial... 
recurrence | familial Bell′s palsy | Bell′s palsy
Web Resource
Rivista di Neurobiologia, ISSN 0035-6336, 1993, Volume 39, Issue 4, pp. 403 - 407
Journal Article
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