Literature DB >> 1456290

Natural history of mosaic trisomy 14 syndrome.

A Fujimoto1, J Allanson, C A Crowe, M H Lipson, V P Johnson.   

Abstract

Trisomy 14 mosaicism produces a distinct phenotype. Among the 13 reported and 2 additional patients, the following findings were present in more than 90%: growth retardation (15/15), psychomotor retardation (10/10), broad nose (13/14), "dysplastic" and/or apparently low-set ears (15/15), micrognathia (15/15), short neck (11/12), congenital heart disease (14/15), and micropenis and cryptorchidism (6/6). Other frequent findings were prominent forehead (12/14), hypertelorism (8/13), narrow palpebral fissure (7/9), large mouth (10/14), cleft or highly arched palate (10/14), body asymmetry (8/12), and abnormal skin pigmentation (6/10). Sex ratio was 6M:9F. Four patients died before age 4 months, while at least 2 patients survived through teens. One boy died at age 3 years following cardiac surgery. One girl with tetralogy of Fallot showed a remarkable improvement in health after Blalock-Taussig procedure. Although the surviving patients showed moderate growth and mental retardation, the oldest surviving woman at 29 years demonstrates functional language and appropriate self help skills.

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Year:  1992        PMID: 1456290     DOI: 10.1002/ajmg.1320440214

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  7 in total

Review 1.  A severely short-statured girl with 47,XX, + 14/46,XX,upd(14)mat, mosaicism.

Authors:  Kikumi Ushijima; Syuichi Yatsuga; Takako Matsumoto; Akie Nakamura; Maki Fukami; Masayo Kagami
Journal:  J Hum Genet       Date:  2018-01-09       Impact factor: 3.172

2.  Outcome of esophageal atresia/tracheoesophageal fistula in extremely low birth weight neonates (<1000 grams).

Authors:  Augusto Zani; Justyna Wolinska; Giovanni Cobellis; Priscilla P L Chiu; Agostino Pierro
Journal:  Pediatr Surg Int       Date:  2015-10-30       Impact factor: 1.827

Review 3.  Current status of human chromosome 14.

Authors:  D Kamnasaran; D W Cox
Journal:  J Med Genet       Date:  2002-02       Impact factor: 6.318

4.  Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

Authors:  S E Antonarakis; J L Blouin; J Maher; D Avramopoulos; G Thomas; C C Talbot
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

5.  Congenital ocular anomaly in an infant with trisomy 14 mosaicism.

Authors:  Jun Ho Choi; Youn Joo Choi; So Young Kim
Journal:  Korean J Ophthalmol       Date:  2012-07-24

6.  Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry.

Authors:  Sarah Okashah; Dhanya Vasudeva; Aya El Jerbi; Houssein Khodjet-El-Khil; Mashael Al-Shafai; Najeeb Syed; Marios Kambouris; Sharda Udassi; Luis R Saraiva; Hesham Al-Saloos; Jai Udassi; Kholoud N Al-Shafai
Journal:  Genes (Basel)       Date:  2022-07-30       Impact factor: 4.141

7.  Complete trisomy 14 mosaicism: first live-born case in Korea.

Authors:  Yun Jung Hur; Taegyu Hwang
Journal:  Korean J Pediatr       Date:  2012-10-29
  7 in total

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