Literature DB >> 17483715

Cleft palate, bilateral external auditory canal atresia, and other midline defects associated with Diamond-Blackfan anemia: case report.

Alicia McFarren1, Somasundaram Jayabose, Mehmet Fevzi Ozkaynak, Oya Tugal, Claudio Sandoval.   

Abstract

Diamond-Blackfan anemia (DBA) is associated with congenital anomalies especially of the midline. When present, facial anomalies are reminiscent of Treacher-Collins syndrome, and both DBA and Treacher-Collins syndrome are disorders of ribosomal biogenesis. Herein, we describe a female infant with multiple midline defects associated with DBA and reaffirm the absence of RPS-19 mutations in DBA patients with facial anomalies.

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Year:  2007        PMID: 17483715     DOI: 10.1097/MPH.0b013e31805d8f45

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  4 in total

1.  Ocular hypertelorism and exotropia as presenting signs in Diamond-Blackfan anemia.

Authors:  Manami Kuze; Hisashi Matsubara; Yukitaka Uji
Journal:  Jpn J Ophthalmol       Date:  2009-01-30       Impact factor: 2.447

2.  Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28.

Authors:  Karen W Gripp; Cynthia Curry; Ann Haskins Olney; Claudio Sandoval; Jamie Fisher; Jessica Xiao-Ling Chong; Lisa Pilchman; Rebecca Sahraoui; Deborah L Stabley; Katia Sol-Church
Journal:  Am J Med Genet A       Date:  2014-06-18       Impact factor: 2.802

3.  Bochdalek hernia with Diamond-Blackfan anemia associated with RPS19 gene mutation: A case report.

Authors:  Ye Seul Yoo; Na Hee Lee; Young Bae Choi
Journal:  Medicine (Baltimore)       Date:  2019-09       Impact factor: 1.817

4.  Surgical treatment of external auditory canal cholesteatoma in congenital malformation of the ear: A case series.

Authors:  Lina Lasminingrum; Sally Mahdiani; Rano Digdayan Makerto
Journal:  Ann Med Surg (Lond)       Date:  2021-09-22
  4 in total

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