Liveborn trisomy 22: report of one case.

S. F. Lean, S. P. Lin, E. Y. Shen, M. Y. Ho, S. Y. Yang

Research output: Contribution to journalReview article

4 Citations (Scopus)

Abstract

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described. Physical manifestations included failure to thrive, hypotonia, pre-auricular sinus, low set ears, hypertelorism, posterior low hair line, micrognathia, cleft palate, congenital heart disease, imperforated anus with anovulvar fistula, contracted pelvis and bilateral rocker-bottom feet. The infant died at two months of age. Cases of trisomy 22 usually present with many severe malformations, and they rarely survive to term. A review of the literature is presented to delineate this chromosome disorder.

Original languageEnglish
Pages (from-to)226-230
Number of pages5
JournalZhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui
Volume33
Issue number3
Publication statusPublished - Jan 1 1992
Externally publishedYes

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Micrognathism
Chromosome Disorders
Hypertelorism
Failure to Thrive
Muscle Hypotonia
Anal Canal
Cleft Palate
Pelvis
Hair
Fistula
Ear
Heart Diseases
Trisomy Chromosome 22
Congenital Vertical talus

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Liveborn trisomy 22 : report of one case. / Lean, S. F.; Lin, S. P.; Shen, E. Y.; Ho, M. Y.; Yang, S. Y.

In: Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui, Vol. 33, No. 3, 01.01.1992, p. 226-230.

Research output: Contribution to journalReview article

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