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Child's Nervous System, ISSN 0256-7040, 5/2018, Volume 34, Issue 5, pp. 911 - 917
The objectives of this study were to evaluate the demographic and clinical characteristics, causes, treatment patterns, outcome, and recurrence of childhood... 
Recurrence | Neurosciences | Medicine & Public Health | Bell’s palsy | Outcome | Facial nerve | Neurosurgery | SURGERY | MANAGEMENT | BELLS-PALSY | PREDNISOLONE | CLINICAL NEUROLOGY | CHILDREN | NERVE PARALYSIS | MELKERSSON-ROSENTHAL-SYNDROME | PEDIATRICS | HYPERTENSION | Bell's palsy | Index Medicus
Journal Article
Plastic and Reconstructive Surgery, ISSN 0032-1052, 10/2016, Volume 138, Issue 4, pp. 879 - 887
Journal Article
Çukurova Üniversitesi Tıp Fakültesi Dergisi, ISSN 0250-5150, 08/2014, Volume 39, Issue 4, pp. 918 - 921
Melkersson-Rosenthal syndrome (MRS) is a rare neuromucocutaneous syndrome characterized by recurrent facial paralysis, orofacial edema and fissured tongue.... 
Melkersson-Rosenthal syndrome | recurrent facial paralysis | children
Journal Article
Journal of Investigational Allergology & Clinical Immunology, ISSN 1018-9068, 01/2018, Volume 28, Issue 4, p. 255
Angioedema involves rapid swelling of the skin, which typically lasts no more than 5-7 days. The affected tissues return to normal with no sequelae. Some... 
Buccal mucosa | Edema | Melkersson-Rosenthal syndrome | Complications | Angioedema | Diabetes mellitus | Hypersensitivity | Mucosa | Hyperplasia | Dyslipidemia | Biopsy | Allergic rhinitis | Skin | Paralysis | Bell's palsy
Journal Article
Journal of Clinical and Analytical Medicine, ISSN 1309-0720, 01/2016, Volume 6, Issue 152, pp. 415 - 417
Melkersson%u2013Rosenthal syndrome is characterized by a triad of symptoms consisting recurring facial paralysis unilateral or bilateral, orofacial edema... 
Lingua plicata | Melkersson-Rosenthal Syndrome | Orofacial edema
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 06/2019, Volume 62, Issue 6, pp. 103536 - 103536
Melkersson Rosenthal syndromes (MRS) is a rare autosomal dominantly inherited neurocutaneous syndrome characterised by a triad of facial (seventh cranial)... 
Melkersson Rosenthal syndrome | SLC27A1 | Orofacial swelling | FATP1 | Fissured tongue | Facial nerve palsy | Phenotype | Humans | Middle Aged | Adolescent | Adult | Female | Male | Child | Melkersson-Rosenthal Syndrome - pathology | Fatty Acid Transport Proteins - genetics | Genetic Heterogeneity | Melkersson-Rosenthal Syndrome - genetics | Index Medicus
Journal Article
European Journal of General Medicine, ISSN 1304-3889, 2015, Volume 12, Issue 1, pp. 78 - 81
Journal Article
Journal Article
Journal Article
Journal Article
Nederlands tijdschrift voor geneeskunde, ISSN 0028-2162, 2016, Volume 160, p. D427
Melkersson-Rosenthal syndrome (MRS) is a relatively rare syndrome characterised by the clinical triad of persisting or recurrent facial oedema, recurrent... 
Recurrence | Humans | Adult | Male | Melkersson-Rosenthal Syndrome - diagnosis | Facial Paralysis - etiology | Melkersson-Rosenthal Syndrome - complications
Journal Article
Clinical and Experimental Dermatology, ISSN 0307-6938, 12/2017, Volume 42, Issue 8, pp. 887 - 889
Journal Article
Çağdaş Tıp Dergisi, ISSN 2146-4189, 03/2012, Volume 2, Issue 1, pp. 26 - 29
Melkersson Rosenthal Syndrome (MRS) is a rarely seen syndrome with unknown etiology. It is described with a classic triad as recurrent facial paralysis,... 
Melkersson Rosenthal Syndrome; facial paralysis
Journal Article
Alergia Astma Immunologia, ISSN 1427-3101, 2015, Volume 20, Issue 2, pp. 117 - 119
Journal Article
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