Literature DB >> 27617157

Thoracic Hypoplasia at Birth as Presenting Feature of Shwachman-Diamond Syndrome in Twins.

Letizia Capasso1, Angela Carla Borrelli1, Julia Cerullo1, Maria Rosaria Pirozzi1, Francesco Raimondi1.   

Abstract

Shwachman-Diamond syndrome (SDS) is a rare autosomal recessive disorder of marrow failure syndrome and exocrine pancreatic dysfunction with an estimated incidence of 1/76,000. When present, characteristic skeletal abnormalities are strongly suggestive of SDS but most often they are seen during childhood and adolescence. We present a case of preterm twins with prenatal diagnosis of thoracic hypoplasia and a clinical evolution that lead to an early diagnosis of SDS. This report highlights the importance of a high index of suspicion for SDS in case of neonatal thoracic hypoplasia.

Entities:  

Keywords:  exocrine pancreatic dysfunction; limb shortness; neutropenia; newborn; thoracic hypoplasia

Year:  2016        PMID: 27617157      PMCID: PMC4999326          DOI: 10.1055/s-0036-1584307

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  14 in total

1.  Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.

Authors:  S Goobie; M Popovic; J Morrison; L Ellis; H Ginzberg; G R Boocock; N Ehtesham; C Bétard; C G Brewer; N M Roslin; T J Hudson; K Morgan; T M Fujiwara; P R Durie; J M Rommens
Journal:  Am J Hum Genet       Date:  2001-03-15       Impact factor: 11.025

Review 2.  Shwachman-diamond syndrome.

Authors:  Yigal Dror; Melvin H Freedman
Journal:  Br J Haematol       Date:  2002-09       Impact factor: 6.998

3.  Pancreatic exocrine enzyme deficiency associated with asphyxiating thoracic dystrophy.

Authors:  M Karjoo; C E Koop; D Cornfeld; P G Holtzapple
Journal:  Arch Dis Child       Date:  1973-02       Impact factor: 3.791

4.  Syndrome of pancreatic insufficiency, blood dyscrasia and metaphyseal dysplasia.

Authors:  E M Pringle; W F Young; E M Haworth
Journal:  Proc R Soc Med       Date:  1968-08

5.  Jeune syndrome associated with pancreatic fibrosis.

Authors:  M Georgiou-Theodoropoulos; M Agapitos; P Theodoropoulos; A Koutselinis
Journal:  Pediatr Pathol       Date:  1988

6.  Shwachman syndrome: unusual presentation as asphyxiating thoracic dystrophy.

Authors:  V V Michels; G K Donovan
Journal:  Birth Defects Orig Artic Ser       Date:  1982

7.  Variable clinical presentation of Shwachman-Diamond syndrome: update from the North American Shwachman-Diamond Syndrome Registry.

Authors:  Kasiani C Myers; Audrey Anna Bolyard; Barbara Otto; Trisha E Wong; Amanda T Jones; Richard E Harris; Stella M Davies; David C Dale; Akiko Shimamura
Journal:  J Pediatr       Date:  2013-12-31       Impact factor: 4.406

8.  The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA.

Authors:  Karthik A Ganapathi; Karyn M Austin; Chung-Sheng Lee; Anusha Dias; Maggie M Malsch; Robin Reed; Akiko Shimamura
Journal:  Blood       Date:  2007-05-02       Impact factor: 22.113

9.  Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome.

Authors:  Andrew J Finch; Christine Hilcenko; Nicolas Basse; Lesley F Drynan; Beatriz Goyenechea; Tobias F Menne; Africa González Fernández; Paul Simpson; Clive S D'Santos; Mark J Arends; Jean Donadieu; Christine Bellanné-Chantelot; Michael Costanzo; Charles Boone; Andrew N McKenzie; Stefan M V Freund; Alan J Warren
Journal:  Genes Dev       Date:  2011-05-01       Impact factor: 11.361

10.  The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast.

Authors:  Tobias F Menne; Beatriz Goyenechea; Nuria Sánchez-Puig; Chi C Wong; Louise M Tonkin; Philip J Ancliff; Renée L Brost; Michael Costanzo; Charles Boone; Alan J Warren
Journal:  Nat Genet       Date:  2007-03-11       Impact factor: 38.330

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  1 in total

1.  A Case of Shwachman-Diamond Syndrome who Presented with Hypotonia.

Authors:  Zeren Barış; Figen Özçay; Lale Olcay; Serdar Ceylaner; Taner Sezer
Journal:  J Pediatr Genet       Date:  2018-03-07
  1 in total

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