Literature DB >> 15889419

Another case of interstitial del(12) involving the proposed cardio-facio-cutaneous candidate region.

Paul A James1, Paul Oei, Daniel Ng, Peter Kannu, Salim Aftimos.   

Abstract

Recent reports of patients with interstitial deletions involving the long arm of chromosome 12 have led to the proposal of a candidate region for the cardio-facio-cutaneous syndrome (CFCS) at (12)(q21.2q22). We now report a patient with an interstitial deletion, del(12)(q21.1q21.3) that overlaps the proposed critical region. The patient is an 11-year-old female with developmental delay. Her growth was normal but she is microcephalic with low set ears. In common with other patients with deletions in this region, she had fine, sparse head and eyebrow hair and a hyperkeratotic follicular rash, which involved her face and limbs. She does not have the diagnostic features of the CFC syndrome. Copyright (c) 2005 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2005        PMID: 15889419     DOI: 10.1002/ajmg.a.30693

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

1.  Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions.

Authors:  Sarah Vergult; Danijela Krgovic; Bart Loeys; Stanislas Lyonnet; Agne Liedén; Britt-Marie Anderlid; Freddie Sharkey; Shelagh Joss; Geert Mortier; Björn Menten
Journal:  Eur J Hum Genet       Date:  2011-04-20       Impact factor: 4.246

2.  De novo variants in ATP2B1 lead to neurodevelopmental delay.

Authors:  Meer Jacob Rahimi; Nicole Urban; Meret Wegler; Heinrich Sticht; Michael Schaefer; Bernt Popp; Frank Gaunitz; Manuela Morleo; Vincenzo Nigro; Silvia Maitz; Grazia M S Mancini; Claudia Ruivenkamp; Eun-Kyung Suk; Tobias Bartolomaeus; Andreas Merkenschlager; Daniel Koboldt; Dennis Bartholomew; Alexander P A Stegmann; Margje Sinnema; Irma Duynisveld; Ramona Salvarinova; Simone Race; Bert B A de Vries; Aurélien Trimouille; Sophie Naudion; Daphna Marom; Uri Hamiel; Noa Henig; Florence Demurger; Nils Rahner; Enrika Bartels; J Austin Hamm; Abbey M Putnam; Richard Person; Rami Abou Jamra; Henry Oppermann
Journal:  Am J Hum Genet       Date:  2022-03-30       Impact factor: 11.043

3.  A New 12q21 Deletion Syndrome: A Case Report and Literature Review.

Authors:  Alessandra Di Nora; Greta De Costa; Alessia Di Mari; Marco Montemagno; Vito Pavone; Piero Pavone
Journal:  Glob Med Genet       Date:  2022-07-21
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.