Unknown

Dataset Information

0

The attenuated end of the phenotypic spectrum in MPS III: from late-onset stable cognitive impairment to a non-neuronopathic phenotype.


ABSTRACT: BACKGROUND:The phenotypic spectrum of many rare disorders is much wider than previously considered. Mucopolysaccharidosis type III (Sanfilippo syndrome, MPS III), is a lysosomal storage disorder traditionally considered to be characterized by childhood onset, progressive neurocognitive deterioration with a rapidly or slowly progressing phenotype. The presented MPS III case series demonstrates adult onset phenotypes with mild cognitive impairment or non-neuronopathic phenotypes. METHODS:In this case series all adult MPS III patients with a mild- or non-neuronopathic phenotype, who attend the outpatient clinic of 3 expert centers for lysosomal storage disorders were included. A mild- or non-neuronopathic phenotype was defined as having completed regular secondary education and attaining a level of independency during adulthood, involving either independent living or a paid job. RESULTS:Twelve patients from six families, with a median age at diagnosis of 43?years (range 3-68) were included (11 MPS IIIA, 1 MPS IIIB). In the four index patients symptoms which led to diagnostic studies (whole exome sequencing and metabolomics) resulting in the diagnosis of MPS III; two patients presented with retinal dystrophy, one with hypertrophic cardiomyopathy and one with neurocognitive decline. The other eight patients were diagnosed by family screening. At a median age of 47?years (range 19-74) 9 out of the 12 patients had normal cognitive functions. Nine patients had retinal dystrophy and 8 patients hypertrophic cardiomyopathy. CONCLUSION:We show the very mild end of the phenotypic spectrum of MPS III, ranging from late-onset stable neurocognitive impairment to a fully non-neuronopathic phenotype. Awareness of this phenotype could lead to timely diagnosis and genetic counseling.

SUBMITTER: Nijmeijer SCM 

PROVIDER: S-EPMC6852993 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

The attenuated end of the phenotypic spectrum in MPS III: from late-onset stable cognitive impairment to a non-neuronopathic phenotype.

Nijmeijer Stephanie C M SCM   van den Born L Ingeborg LI   Kievit Anneke J A AJA   Stepien Karolina M KM   Langendonk Janneke J   Marchal Jan Pieter JP   Roosing Susanne S   Wijburg Frits A FA   Wagenmakers Margreet A E M MAEM  

Orphanet journal of rare diseases 20191112 1


<h4>Background</h4>The phenotypic spectrum of many rare disorders is much wider than previously considered. Mucopolysaccharidosis type III (Sanfilippo syndrome, MPS III), is a lysosomal storage disorder traditionally considered to be characterized by childhood onset, progressive neurocognitive deterioration with a rapidly or slowly progressing phenotype. The presented MPS III case series demonstrates adult onset phenotypes with mild cognitive impairment or non-neuronopathic phenotypes.<h4>Method  ...[more]

Similar Datasets

| S-EPMC8248480 | biostudies-literature
| S-EPMC7432645 | biostudies-literature
| S-EPMC7203653 | biostudies-literature
| S-EPMC4140763 | biostudies-literature
| S-EPMC4624020 | biostudies-literature
| S-EPMC3977613 | biostudies-literature
| S-EPMC8543298 | biostudies-literature
| S-EPMC7409508 | biostudies-literature
| S-EPMC7898319 | biostudies-literature
| S-EPMC5125779 | biostudies-literature