Literature DB >> 8121193

Developmental disorders of the lymphatic system.

R Greenlee1, H Hoyme, M Witte, P Crowe, C Witte.   

Abstract

Approximately 67% of human conceptuses die prenatally. Of these, a significant number involve a disorder of the lymphatic system. A small number of live-born children also exhibit congenital lymphatic malformations, including an estimated 60% of patients with Turner syndrome. These observations have prompted a search for the genetic and dysmorphologic basis and the different patterns of congenital lymphedema and associated anomalies. In this article, we attempt to summarize available pertinent information on congenital disorders of the lymphatic system and to propose a conceptual overview of lymphatic development.

Entities:  

Mesh:

Year:  1993        PMID: 8121193

Source DB:  PubMed          Journal:  Lymphology        ISSN: 0024-7766            Impact factor:   1.286


  10 in total

1.  Primary lymphedema tarda in an 88-year-old African-American male.

Authors:  Ahmed Faraz Aslam; Ahmad Kamal Aslam; Muhammad Umair R Qamar; Robert Levey
Journal:  J Natl Med Assoc       Date:  2005-07       Impact factor: 1.798

2.  Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3.

Authors:  Ronen Spiegel; Arash Ghalamkarpour; Etty Daniel-Spiegel; Miikka Vikkula; Stavit A Shalev
Journal:  J Hum Genet       Date:  2006-08-19       Impact factor: 3.172

3.  Plastic bronchitis in children with Fontan palliation: analogue to protein losing enteropathy?

Authors:  B Stiller; F Riedel; K Paul; F K H van Landeghem
Journal:  Pediatr Cardiol       Date:  2002 Jan-Feb       Impact factor: 1.655

4.  Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration Family.

Authors:  Debbie J Mustacich; Li-Wen Lai; Michael J Bernas; Jazmine A Jones; Reginald J Myles; Phillip H Kuo; Walter H Williams; Charles L Witte; Robert P Erickson; Marlys Hearst Witte
Journal:  Am J Med       Date:  2021-10-15       Impact factor: 4.965

5.  Mapping of primary congenital lymphedema to the 5q35.3 region.

Authors:  A L Evans; G Brice; V Sotirova; P Mortimer; J Beninson; K Burnand; J Rosbotham; A Child; M Sarfarazi
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

Review 6.  Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132

7.  Congenital lymphatic hypoplasia in unilateral lower limb with abnormal technetium-99m sulphur colloid uptake in both breasts.

Authors:  Subramanyam Padma; Palaniswamy Shanmuga Sundaram
Journal:  Indian J Nucl Med       Date:  2014-10

8.  Primary congenital lymphedema complicated by hydrops fetalis: a case report and review of the literature.

Authors:  Paul Singh; Matthew Connell
Journal:  Case Rep Obstet Gynecol       Date:  2013-02-28

9.  Transient idiopathic primary penoscrotal edema.

Authors:  Sody A Namir; Akiva Trattner
Journal:  Indian J Dermatol       Date:  2013-09       Impact factor: 1.494

Review 10.  A Primer on a Comprehensive Genetic Approach to Vascular Anomalies.

Authors:  Alexandra J Borst; Taizo A Nakano; Francine Blei; Denise M Adams; Jessica Duis
Journal:  Front Pediatr       Date:  2020-10-19       Impact factor: 3.418

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.