Literature DB >> 10651712

Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphy.

J L Rosbotham1, G W Brice, A H Child, T O Nunan, P S Mortimer, K G Burnand.   

Abstract

Distichiasis-lymphoedema is a rare variant of the genetically determined lymphoedemas; distichiasis is the abnormal development of the meibomian glands causing aberrant growth of eyelashes. However, a better understanding of this clinically distinct subgroup may provide useful information on the genetic inheritance of all types of lymphoedema. This report provides phenotype data on a very large family with distichiasis-lymphoedema. Lymphoscintigraphy and light reflection rheography (venous function) were undertaken to identify the phenotype more clearly. As a result of lymphoscintigraphy several subjects were reclassified phenotypically (unaffected or affected) with implications for genetic linkage studies. Associated congenital abnormalities were found and venous abnormalities were almost always present in affected limbs. A dominant inheritance with incomplete penetrance was confirmed.

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Mesh:

Year:  2000        PMID: 10651712     DOI: 10.1046/j.1365-2133.2000.03258.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  6 in total

1.  Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs.

Authors:  M Y M Ng; T Andrew; T D Spector; S Jeffery
Journal:  J Med Genet       Date:  2005-03       Impact factor: 6.318

2.  Mutations in EPHB4 cause human venous valve aplasia.

Authors:  Oliver Lyons; James Walker; Christopher Seet; Mohammed Ikram; Adam Kuchta; Andrew Arnold; Magda Hernández-Vásquez; Maike Frye; Gema Vizcay-Barrena; Roland A Fleck; Ashish S Patel; Soundrie Padayachee; Peter Mortimer; Steve Jeffery; Siren Berland; Sahar Mansour; Pia Ostergaard; Taija Makinen; Bijan Modarai; Prakash Saha; Alberto Smith
Journal:  JCI Insight       Date:  2021-09-22

3.  Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.

Authors:  G Brice; S Mansour; R Bell; J R O Collin; A H Child; A F Brady; M Sarfarazi; K G Burnand; S Jeffery; P Mortimer; V A Murday
Journal:  J Med Genet       Date:  2002-07       Impact factor: 6.318

4.  Imbalance between Expression of FOXC2 and Its lncRNA in Lymphedema-Distichiasis Caused by Frameshift Mutations.

Authors:  Sara Missaglia; Daniela Tavian; Sandro Michelini; Paolo Enrico Maltese; Andrea Bonanomi; Matteo Bertelli
Journal:  Genes (Basel)       Date:  2021-04-27       Impact factor: 4.096

5.  Human venous valve disease caused by mutations in FOXC2 and GJC2.

Authors:  Oliver Lyons; Prakash Saha; Christopher Seet; Adam Kuchta; Andrew Arnold; Steven Grover; Victoria Rashbrook; Amélie Sabine; Gema Vizcay-Barrena; Ash Patel; Francesca Ludwinski; Soundrie Padayachee; Tsutomu Kume; Brenda R Kwak; Glen Brice; Sahar Mansour; Pia Ostergaard; Peter Mortimer; Steve Jeffery; Nigel Brown; Taija Makinen; Tatiana V Petrova; Bijan Modarai; Alberto Smith
Journal:  J Exp Med       Date:  2017-08-07       Impact factor: 14.307

6.  A Novel Mutation in the FOXC2 Gene: A Heterozygous Insertion of Adenosine (c.867insA) in a Family with Lymphoedema of Lower Limbs without Distichiasis.

Authors:  Tanja Planinsek Rucigaj; Matija Rijavec; Jovan Miljkovic; Julij Selb; Peter Korosec
Journal:  Radiol Oncol       Date:  2017-07-06       Impact factor: 2.991

  6 in total

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