Liveborn trisomy 22: report of one case.

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

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 journal › Review article › peer-review

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 language	English
Pages (from-to)	226-230
Number of pages	5
Journal	Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui
Volume	33
Issue number	3
Publication status	Published - Jan 1 1992
Externally published	Yes

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

Cite this

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title = "Liveborn trisomy 22: report of one case.",

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.",

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AU - Lean, S. F.

AU - Lin, S. P.

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AU - Ho, M. Y.

AU - Yang, S. Y.

PY - 1992/1/1

Y1 - 1992/1/1

N2 - 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.

AB - 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.

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Liveborn trisomy 22: report of one case.

Abstract

ASJC Scopus subject areas

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