The phenotypic spectrum of duplication 5q35.2–q35.3 encompassing NSD1: Is it really a reversed sotos syndrome?. Issue 9 (2nd August 2013)
- Record Type:
- Journal Article
- Title:
- The phenotypic spectrum of duplication 5q35.2–q35.3 encompassing NSD1: Is it really a reversed sotos syndrome?. Issue 9 (2nd August 2013)
- Main Title:
- The phenotypic spectrum of duplication 5q35.2–q35.3 encompassing NSD1: Is it really a reversed sotos syndrome?
- Authors:
- Dikow, Nicola
Maas, Bianca
Gaspar, Harald
Kreiss‐Nachtsheim, Martina
Engels, Hartmut
Kuechler, Alma
Garbes, Lutz
Netzer, Christian
Neuhann, Teresa M.
Koehler, Udo
Casteels, Kristina
Devriendt, Koen
Janssen, Johannes W.G.
Jauch, Anna
Hinderhofer, Katrin
Moog, Ute - Abstract:
- Abstract: Loss‐of‐function mutations of NSD1 and 5q35 microdeletions encompassing NSD1 are a major cause of Sotos syndrome (Sos), which is characterized by overgrowth, macrocephaly, characteristic facies, and variable intellectual disability (ID). Microduplications of 5q35.2–q35.3 including NSD1 have been reported in only five patients so far and described clinically as a reversed Sos resulting from a hypothetical gene dosage effect of NSD1 . Here, we report on nine patients from five families with interstitial duplication 5q35 including NSD1 detected by molecular karyotyping. The clinical features of all 14 individuals are reviewed. Patients with microduplications including NSD1 appear to have a consistent phenotype consisting of short stature, microcephaly, learning disability or mild to moderate ID, and distinctive facial features comprising periorbital fullness, short palpebral fissures, a long nose with broad or long nasal tip, a smooth philtrum and a thin upper lip vermilion. Behavioral problems, ocular and minor hand anomalies may be associated. Based on our findings, we discuss the possible etiology and conclude that it is possible, but so far unproven, that a gene dosage effect of NSD1 may be the major cause. © 2013 Wiley Periodicals, Inc.
- Is Part Of:
- American journal of medical genetics. Volume 161:Issue 9(2013:Sep.)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 161:Issue 9(2013:Sep.)
- Issue Display:
- Volume 161, Issue 9 (2013)
- Year:
- 2013
- Volume:
- 161
- Issue:
- 9
- Issue Sort Value:
- 2013-0161-0009-0000
- Page Start:
- 2158
- Page End:
- 2166
- Publication Date:
- 2013-08-02
- Subjects:
- microduplication 5q35 -- NSD1 -- partial trisomy 5q -- gene dosage -- Sotos syndrome
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.36046 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8987.xml