Literature DB >> 15817983

Fanconi's anemia in newborn.

Tushar B Parikh1, Rekha H Udani, Ruchi N Nanavati, Babu Rao.   

Abstract

Fanconi's anemia (FA) is a paradigm for congenital anomalies, aplastic anemia and predisposition to malignancies. Identification of the disease at birth is based on characteristic physical malformations, as hematologic manifestations at birth are extremely rare. We report a case of FA in a newborn who presented with anophthalmia, unilateral radial ray defect, hemivertebrae and thrombocytopenia.

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Year:  2005        PMID: 15817983

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  4 in total

1.  Fanconi anemia in infancy: report of hematopoietic stem cell transplantation to a 13-month-old patient.

Authors:  Koichi Oshima; Akira Kikuchi; Shinji Mochizuki; Daisuke Toyama; Naoki Uchisaka; Miharu Yabe; Ryoji Hanada
Journal:  Int J Hematol       Date:  2009-05-19       Impact factor: 2.490

2.  Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage.

Authors:  Asmin Tulpule; M William Lensch; Justine D Miller; Karyn Austin; Alan D'Andrea; Thorsten M Schlaeger; Akiko Shimamura; George Q Daley
Journal:  Blood       Date:  2010-01-20       Impact factor: 22.113

Review 3.  A case report and literature review of Fanconi Anemia (FA) diagnosed by genetic testing.

Authors:  Ponnumony John Solomon; Priya Margaret; Ramya Rajendran; Revathy Ramalingam; Godfred A Menezes; Alph S Shirley; Seung Jun Lee; Moon-Woo Seong; Sung Sup Park; Dodam Seol; Soo Hyun Seo
Journal:  Ital J Pediatr       Date:  2015-05-08       Impact factor: 2.638

4.  Microphthalmos, orbital cyst, and missing thumbs: A rare case report.

Authors:  Tayyab Afghani; Hassan Mansoor; Waseem Shehzad
Journal:  Oman J Ophthalmol       Date:  2015 Sep-Dec
  4 in total

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