Triple X syndrome with rare phenotypic presentation-Reference-Cited by-同舟云学术

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Triple X syndrome with rare phenotypic presentation

Published:2008-06 Issue:6 Volume:75 Page:629-631
ISSN:0019-5456
Container-title:The Indian Journal of Pediatrics
language:en
Short-container-title:Indian J Pediatr

Author:

Jagadeesh Sujatha,Jabeen Gazala,Bhat Lathaa,Vasikarla Madhavi,Suresh Arvind,Seshadri Suresh,Lata S.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s12098-008-0120-8.pdf

Reference6 articles.

1. Mary GL, Bruce B et al. 47 XXX. What is the Prognosis? Pediatrics 1988; 4: 82.

2. Mai PH, Kathleen SW et al. Case Report of a 22 week Fetus with 47, XXX karyotype and Multiple Lower Mesodermal Defects. Pediatr and Devel Pathol 1999; 2: 58–61.

3. Trautner MC, Aladangady N et al. Jejunal Atresia in an infant with triple — X syndrome. J Matern — Fetal and Neonatal Med 2004; 16: 198–200.

4. Kurtoglu S, Atabek ME et al. Triple — X syndrome accompanied by congenital adrenal hyperplasia: case report. The Turk J Pediatr 2004; 46: 377–379.

5. Hiwaki Y, Isematsu E. Schizencephaly in Triple — X syndrome. Pediatr Int J 2001; 43: 296–299.

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1. Goltz Syndrome Combined with Triple X Syndrome, a Case Report;The Cleft Palate-Craniofacial Journal;2022-11-28

2. Congenital Cataract in a Triple X Syndrome Patient;Journal of the Korean Ophthalmological Society;2020-05-15

3. Triple X Syndrome with a Rare Finding: Cleft Palate;The Journal of Pediatric Research;2018-06-27

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5. Clinico-statistical Study of the Cases of Cleft Lip and/or Palate in the Past 10 Years at Our Department;Yamaguchi Medical Journal;2017-08-01

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