Literature DB >> 761419

Melkersson-Rosenthal's syndrome in four generations.

C Lygidakis, C Tsakanikas, A Ilias, D Vassilopoulos.   

Abstract

Melkersson-Rosenthal's syndrome is a rare condition, the hereditary nature of which is still in dispute. A family with seven affected members in four generations is described, which provides further evidence for the genetic basis of the syndrome.

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Mesh：

Year:  1979        PMID： 761419     DOI： 10.1111/j.1399-0004.1979.tb01760.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  6 in total

1.  Fountain's syndrome: mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips.

Authors:  J P Fryns
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

2.  Oral Crohn's disease: the distinction from the Melkersson-Rosenthal syndrome.

Authors:  T Diamond; P G Patterson; T G Emerson
Journal:  Ulster Med J       Date:  1990-10

Review 3.  Melkersson⁻Rosenthal Syndrome in Childhood: Report of Three Paediatric Cases and a Review of the Literature.

Authors:  Salvatore Savasta; Alessandra Rossi; Thomas Foiadelli; Amelia Licari; Anna Maria Elena Perini; Giovanni Farello; Alberto Verrotti; Gian Luigi Marseglia
Journal:  Int J Environ Res Public Health       Date:  2019-04-10       Impact factor: 3.390

Review 4.  Management Strategies of Melkersson-Rosenthal Syndrome: A Review.

Authors:  Sumeet R Dhawan; Arushi G Saini; Pratibha D Singhi
Journal:  Int J Gen Med       Date:  2020-02-26

Review 5.  Research progress on Melkersson-Rosenthal syndrome.

Authors:  Wenjing Kuang; Xiaobo Luo; Jiongke Wang; Xin Zeng
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2021-04-25

6.  Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling.

Authors:  Babita Kajal; John Harvey; Salem Alowami
Journal:  Diagn Pathol       Date:  2013-11-13       Impact factor: 2.644
  6 in total

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