Literature DB >> 23463902

Focal dermal hypoplasia: updates.

L Wang1, X Jin, X Zhao, D Liu, T Hu, W Li, L Jiang, H Dan, X Zeng, Q Chen.   

Abstract

Focal dermal hypoplasia (FDH), or Goltz-Gorlin syndrome, is a rare syndrome and may result in multisystem disorders. Several reviews of FDH have been published. However, the last comprehensive review of this disorder appeared more than 20 years ago. To date, a number of new clinical manifestations have been reported and considerable knowledge has accumulated regarding etiology and pathogenetic mechanisms. The purpose of this review is to gather these more recent data and to provide organized and reliable information. So we reviewed 159 cases of FDH that had been reported from 1990 to 2012, summarized the new discoveries, and suggested a potential standard for the diagnosis of FDH. We also reported on a Chinese girl with FDH, who was clinically and histologically in accord with FDH, as an example.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  diagnostics; genetics

Mesh:

Year:  2013        PMID: 23463902     DOI: 10.1111/odi.12083

Source DB:  PubMed          Journal:  Oral Dis        ISSN: 1354-523X            Impact factor:   3.511


  8 in total

1.  Multiple requirements of the focal dermal hypoplasia gene porcupine during ocular morphogenesis.

Authors:  Elizabeth J Bankhead; Mary P Colasanto; Kayla M Dyorich; Milan Jamrich; L Charles Murtaugh; Sabine Fuhrmann
Journal:  Am J Pathol       Date:  2014-11-03       Impact factor: 4.307

2.  Focal Dermal Hypoplasia (Goltz Syndrome): A Rare Case.

Authors:  Isha Gupta; Neha Dhankar; Surabhi Dayal; Meha Tyagi
Journal:  Indian Dermatol Online J       Date:  2022-06-24

3.  Goltz-Gorlin Syndrome: Revisiting the Clinical Spectrum.

Authors:  Dhanya Yesodharan; Uta Meyer Zum Büschenfelde; Kerstin Kutsche; K Mohandas Nair; Sheela Nampoothiri
Journal:  Indian J Pediatr       Date:  2018-01-31       Impact factor: 1.967

4.  Focal dermal hypoplasia: A novel finding in disguise.

Authors:  S Nathwani; K Martin; R Bunyan
Journal:  J Oral Biol Craniofac Res       Date:  2018-02-01

Review 5.  Management of Congenital Diaphragmatic Hernia (CDH): Role of Molecular Genetics.

Authors:  Giulia Cannata; Chiara Caporilli; Federica Grassi; Serafina Perrone; Susanna Esposito
Journal:  Int J Mol Sci       Date:  2021-06-14       Impact factor: 5.923

6.  An Unexpected Airway Complication in a Male Patient with Goltz Syndrome.

Authors:  Sadie Smith; Kavita Gadhok; Dmitri Guvakov
Journal:  Case Rep Anesthesiol       Date:  2016-09-18

7.  Focal Dermal Hypoplasia (Goltz Syndrome): A Case Report Showing a Wide Variety of Systemic and Oral Manifestations.

Authors:  Átila Vinícius Vitor Nobre; Mário Taba; Alfredo Ribeiro Silva; Sérgio Luís Scombatti de Souza; Ana Carolina Fragoso Motta
Journal:  Ann Dermatol       Date:  2022-08       Impact factor: 0.722

8.  Goltz syndrome in males: A clinical report of a male patient carrying a novel PORCN variant and a review of the literature.

Authors:  Sofia Frisk; Catherine Grandpeix-Guyodo; Karin Popovic Silwerfeldt; Helgi Thor Hjartarson; Dimitris Chatzianastassiou; Irina Magnusson; Tobias Laurell; Ann Nordgren
Journal:  Clin Case Rep       Date:  2018-09-21
  8 in total

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