LANGER-GIEDION SYNDROME: A DISTINCT PHENOTYPE (LETTERS TO EDITOR)

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GEORGE RIYA; NAJMUDDIN FEHMIDA; RAI RAJESH; LAHIRI KEYA

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Journal Paper

Paper Information

Journal: Iranian Journal of Pediatrics Year:2014 | Volume:24 | Issue:5 Page(s): 656-663

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Information Journal Paper

Title

LANGER-GIEDION SYNDROME: A DISTINCT PHENOTYPE (LETTERS TO EDITOR)

Author(s)

GEORGE RIYA | NAJMUDDIN FEHMIDA | RAI RAJESH | LAHIRI KEYA | Issue Writer Certificate

Keywords

TRICHORHINOPHALANGEAL SYNDROME TYPE II

EXOSTOSES

MICRODELETION

DYSMORPHIC FEATURES

CONTIGUOUS GENE DELETION SYNDROME

Abstract

Trichorhinophalangeal syndrome (TRPS), as the name suggests is a rare genetic disorder which affects the tricho (hair), rhino (nose), phalanges (digits) [1] and has been classified into three types. TRICHORHINOPHALANGEAL SYNDROME TYPE II (TRPS2) is also known as Langer-Giedion syndrome (LGS). It was first described by Andreas Giedion, a Swiss pediatric radiologist and Leonard O Langer Jr, an American radiologist.

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APA: Copy

GEORGE, RIYA, NAJMUDDIN, FEHMIDA, RAI, RAJESH, & LAHIRI, KEYA. (2014). LANGER-GIEDION SYNDROME: A DISTINCT PHENOTYPE (LETTERS TO EDITOR). IRANIAN JOURNAL OF PEDIATRICS, 24(5), 656-663. SID. https://sid.ir/paper/637523/en

Vancouver: Copy

GEORGE RIYA, NAJMUDDIN FEHMIDA, RAI RAJESH, LAHIRI KEYA. LANGER-GIEDION SYNDROME: A DISTINCT PHENOTYPE (LETTERS TO EDITOR). IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2014;24(5):656-663. Available from: https://sid.ir/paper/637523/en

IEEE: Copy

RIYA GEORGE, FEHMIDA NAJMUDDIN, RAJESH RAI, and KEYA LAHIRI, “LANGER-GIEDION SYNDROME: A DISTINCT PHENOTYPE (LETTERS TO EDITOR),” IRANIAN JOURNAL OF PEDIATRICS, vol. 24, no. 5, pp. 656–663, 2014, [Online]. Available: https://sid.ir/paper/637523/en

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