X-linked Hypophosphatemic Rickets, del(2)(q37.1;q37.3) Deletion Syndrome and Mosaic Turner Syndrome, mos 45,X/46,X, del(2)(q37.1;q37.3) in a 3-year-old Female.
10.11005/jbm.2017.24.4.257
- Author:
Alaina P VIDMAR
1
;
Brian MIYAZAKI
;
Pedro A SANCHEZ-LARA
;
Pisit PITUKCHEEWANONT
Author Information
1. Center for Endocrinology, Diabetes and Metabolism, Division of Endocrinology, Children's Hospital Los Angeles, Los Angeles, CA, USA. dpisit@chla.usc.edu
- Publication Type:Case Report
- Keywords:
Bone diseases;
Microarray analysis;
Rickets hypophosphatemic;
Turner syndrome
- MeSH:
Bone Diseases;
Child, Preschool*;
Chromosomes, Human, Pair 2;
Diagnosis;
Familial Hypophosphatemic Rickets*;
Female*;
Gene Deletion;
Genetic Testing;
Humans;
Karyotype;
Microarray Analysis;
Phenotype;
PHEX Phosphate Regulating Neutral Endopeptidase;
Turner Syndrome*
- From:Journal of Bone Metabolism
2017;24(4):257-261
- CountryRepublic of Korea
- Language:English
-
Abstract:
There are currently no published cases that report concomitant Turner syndrome (TS), 2q37 deletion syndrome and X-linked hypophosphatemic rickets (XLH). Interestingly, since the clinical phenotypes of TS and 2q37 deletion syndrome overlap, the correct diagnosis may be missed without a standardized approach to genetic testing consisting of both karyotype and microarray. Both chromosome anomalies have been associated with short stature and a variety of skeletal abnormalities however to date no reports have associated these syndromes in association with a phosphate regulating endopeptidase homolog, X-linked (PHEX) gene deletion resulting in XLH. We report a 3-year-old female with 3 concurrent genetic disorders including a 9.98 Mb terminal deletion of chromosome 2: del(2)(q37.1;q37.3), XLH secondary to a small microdeletion of part of the PHEX gene, and mosaic TS (mos 45,X[32]/46,X[18]). This is the first case report of a patient with 2q37 deletion syndrome and mosaic TS (mos 45,X[32]/46,X[18]) found to have XLH secondary to an interstitial constitutional PHEX gene deletion. Her severe phenotype and multiple genotypic findings reinforce the importance of thorough genetic testing in the setting of complicated phenotypic presentations.
