Literature DB >> 20177377

Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency.

Jean-Luc Dominique Alessandri1, Duksha Ramful, Fabrice Cuillier.   

Abstract

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Year:  2010        PMID： 20177377     DOI： 10.1097/MCD.0b013e328335c14a

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  5 in total

1.  Clinical and radiological pictures of two newborn babies with manifestations of chondrodysplasia punctata and review of available literature.

Authors:  Elżbieta Jurkiewicz; Beata Marcinska; Joanna Bothur-Nowacka; Anna Dobrzanska
Journal:  Pol J Radiol       Date:  2013-04

2.  A case of rhizomelic chondrodysplasia punctata in newborn.

Authors:  Nalan Karabayır; Gonca Keskindemirci; Erdal Adal; Orhan Korkmaz
Journal:  Case Rep Med       Date:  2014-03-09

3.  Vitamin K Deficiency Embryopathy from Hyperemesis Gravidarum.

Authors:  Andrew S Lane; Jennifer L Stallworth; Kacey Y Eichelberger; Kenneth F Trofatter
Journal:  Case Rep Obstet Gynecol       Date:  2015-08-12

4.  Rare Case of Rhizomelic Chondrodysplasia Punctata.

Authors:  Yashwant Mahale; Vikram V Kadu; Amit Chaudhari
Journal:  J Orthop Case Rep       Date:  2015 Jul-Sep

5.  Hyperemesis gravidarum and vitamin K deficiency: a systematic review.

Authors:  Kelly Nijsten; Loïs van der Minnen; Hanke M G Wiegers; Marjette H Koot; Saskia Middeldorp; Tessa J Roseboom; Iris J Grooten; Rebecca C Painter
Journal:  Br J Nutr       Date:  2021-07-30       Impact factor: 4.125
  5 in total

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