Literature DB >> 9555587

Diaphragmatic hernia in the Coffin-Siris syndrome.

V Delvaux1, P Moerman, J P Fryns.   

Abstract

At 32 weeks of gestation, delivery of a female fetus was induced because of severe malformations seen on ultrasonogram: congenital diaphragmatic hernia and cerebellar hypoplasia. The diagnosis of Coffin-Siris syndrome was based on the physical examination: coarse face with low-set ears, low nuchal hairline, scalp hypotrichosis and hypoplasia of the nails of fingers and toes with absence of the right fifth fingernail. Autopsy confirmed the prenatally diagnosed major associated abnormalities: hypoplasia of the cerebellum and congenital diaphragmatic hernia. Various clinical entities are included in the differential diagnosis.

Entities:  

Mesh:

Year:  1998        PMID: 9555587

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  7 in total

1.  The Coffin-Siris syndrome: a proposed diagnostic approach and assessment of 15 overlapping cases.

Authors:  Samantha A Schrier; Joann N Bodurtha; Barbara Burton; Albert E Chudley; Mary Anne D Chiong; Maria Gabriella D'avanzo; Sally Ann Lynch; Antonio Musio; Dmitriy M Nyazov; Pedro A Sanchez-Lara; Stavit A Shalev; Matthew A Deardorff
Journal:  Am J Med Genet A       Date:  2012-06-18       Impact factor: 2.802

2.  Fryns syndrome a presentation of two siblings with congenital diaphragmatic hernia.

Authors:  Mohammed Joudi Aboud; Mohammed Mojar Al-Shamsy
Journal:  Pediatr Surg Int       Date:  2011-06       Impact factor: 1.827

3.  Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data.

Authors:  Amy Hardcastle; Aliska M Berry; Ian M Campbell; Xiaonan Zhao; Pengfei Liu; Amanda E Gerard; Jill A Rosenfeld; Saumya D Sisoudiya; Andres Hernandez-Garcia; Sara Loddo; Silvia Di Tommaso; Antonio Novelli; Maria L Dentici; Rossella Capolino; Maria C Digilio; Ludovico Graziani; Cecilie F Rustad; Katherine Neas; Giovanni B Ferrero; Alfredo Brusco; Eleonora Di Gregorio; Diana Wellesley; Claire Beneteau; Madeleine Joubert; Kris Van Den Bogaert; Anneleen Boogaerts; Dominic J McMullan; John Dean; Maria G Giuffrida; Laura Bernardini; Vinod Varghese; Nora L Shannon; Rachel E Harrison; Wayne W K Lam; Shane McKee; Peter D Turnpenny; Trevor Cole; Jenny Morton; Jacqueline Eason; Marilyn C Jones; Rebecca Hall; Michael Wright; Karen Horridge; Chad A Shaw; Wendy K Chung; Daryl A Scott
Journal:  Am J Med Genet A       Date:  2022-07-29       Impact factor: 2.578

Review 4.  Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia.

Authors:  Yoel Gofin; Xiaonan Zhao; Amanda Gerard; Fernando Scaglia; Michael F Wangler; Samantha A Schrier Vergano; Daryl A Scott
Journal:  Am J Med Genet A       Date:  2022-07-07       Impact factor: 2.578

5.  Prenatal diagnosis of congenital diaphragmatic hernia in a fetus with 46,XY/46,X,-Y,+der(Y)t(Y;1)(q12;q12) mosaicism: a case report.

Authors:  Hyun Young Ahn; Jong Chul Shin; Yeon Hee Kim; Hyun Sun Ko; In Yang Park; Sa Jin Kim; Jong Gu Rha; Soo Pyung Kim
Journal:  J Korean Med Sci       Date:  2005-10       Impact factor: 2.153

6.  Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH.

Authors:  Tiana M Scott; Ian M Campbell; Andres Hernandez-Garcia; Seema R Lalani; Pengfei Liu; Chad A Shaw; Jill A Rosenfeld; Daryl A Scott
Journal:  J Med Genet       Date:  2021-01-18       Impact factor: 6.318

7.  Prenatal presentation of multiple anomalies associated with haploinsufficiency for ARID1A.

Authors:  Anne Slavotinek; Mathilde Lefebvre; Anne-Claire Brehin; Christel Thauvin; Sophie Patrier; Teresa N Sparks; Mary Norton; Jingwei Yu; Eric Huang
Journal:  Eur J Med Genet       Date:  2021-12-20       Impact factor: 2.465

  7 in total

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