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A very rare case of a newborn with tetrasomy 9p and literature review

A very rare case of a newborn with tetrasomy 9p and literature review

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_44d5270247fb4cb5a43aa8e4e90369ba

A very rare case of a newborn with tetrasomy 9p and literature review

About this item

Full title

A very rare case of a newborn with tetrasomy 9p and literature review

Publisher

Ankara: Akdema Informatics and Publishing

Journal title

Turkish journal of pediatrics, 2022-01, Vol.64 (1), p.171-178

Language

English

Formats

Publication information

Publisher

Ankara: Akdema Informatics and Publishing

More information

Scope and Contents

Contents

Background. Tetrasomy 9p is a rare genetic condition which usually results from a supernumerary isochromosome derived from the short arm of chromosome 9. Phenotypic findings include multiple congenital anomalies, facial dysmorphism, growth and developmental delays, and also vary according to the presence and degree of mosaicism.
Case. We report...

Alternative Titles

Full title

A very rare case of a newborn with tetrasomy 9p and literature review

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_44d5270247fb4cb5a43aa8e4e90369ba

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_44d5270247fb4cb5a43aa8e4e90369ba

Other Identifiers

ISSN

0041-4301

E-ISSN

2791-6421

DOI

10.24953/turkjped.2021.685

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