Hendriksz, Christian J. and Anheim, Mathieu and Bauer, Peter and Bonnot, Olivier and Chakrapani, Anupam and Corvol, Jean-Christophe and de Koning, Tom J. and Degtyareva, Anna and Dionisi-Vici, Carlo and Doss, Sarah and Duning, Thomas and Giunti, Paola and Iodice, Rosa and Johnston, Tracy and Kelly, Dierdre and Kluenemann, Hans-Hermann and Lorenzl, Stefan and Padovani, Alessandro and Pocovi, Miguel and Synofzik, Matthis and Terblanche, Alta and Bergh, Florian Then and Topcu, Meral and Tranchant, Christine and Walterfang, Mark and Velten, Christian and Kolb, Stefan A. (2017) The hidden Niemann-Pick type C patient: clinical niches for a rare inherited metabolic disease. CURRENT MEDICAL RESEARCH AND OPINION, 33 (5). pp. 877-890. ISSN 0300-7995, 1473-4877
Full text not available from this repository. (Request a copy)Abstract
Background: Niemann-Pick disease type C (NP-C) is a rare, inherited neurodegenerative disease of impaired intracellular lipid trafficking. Clinical symptoms are highly heterogeneous, including neurological, visceral, or psychiatric manifestations. The incidence of NP-C is under-estimated due to under-recognition or misdiagnosis across a wide range of medical fields. New screening and diagnostic methods provide an opportunity to improve detection of unrecognized cases in clinical sub-populations associated with a higher risk of NP-C. Patients in these at-risk groups (clinical niches) have symptoms that are potentially related to NP-C, but go unrecognized due to other, more prevalent clinical features, and lack of awareness regarding underlying metabolic causes. Methods: Twelve potential clinical niches identified by clinical experts were evaluated based on a comprehensive, non-systematic review of literature published to date. Relevant publications were identified by targeted literature searches of EMBASE and PubMed using key search terms specific to each niche. Articles published in English or other European languages up to 2016 were included. Findings: Several niches were found to be relevant based on available data: movement disorders (early-onset ataxia and dystonia), organic psychosis, early-onset cholestasis/(hepato)splenomegaly, cases with relevant antenatal findings or fetal abnormalities, and patients affected by family history, consanguinity, and endogamy. Potentially relevant niches requiring further supportive data included: early-onset cognitive decline, frontotemporal dementia, parkinsonism, and chronic inflammatory CNS disease. There was relatively weak evidence to suggest amyotrophic lateral sclerosis or progressive supranuclear gaze palsy as potential niches. Conclusions: Several clinical niches have been identified that harbor patients at increased risk of NP-C.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | LYSOSOMAL STORAGE DISORDERS; PROGRESSIVE SUPRANUCLEAR PALSY; AMYOTROPHIC-LATERAL-SCLEROSIS; FRONTOTEMPORAL LOBAR DEGENERATION; HEXANUCLEOTIDE REPEAT EXPANSION; GENOTYPE-PHENOTYPE CORRELATIONS; SUSPECTED MULTIPLE-SCLEROSIS; RECESSIVE CEREBELLAR ATAXIAS; SCHIZOPHRENIA-LIKE PSYCHOSIS; EARLY-ONSET ATAXIA; Niemann-Pick disease type C (NP-C); Diagnosis; Screening; Clinical niche; Differential diagnosis; Epidemiology; Inborn errors of metabolism (IEM) |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Lehrstuhl für Psychiatrie und Psychotherapie |
| Depositing User: | Petra Gürster |
| Date Deposited: | 14 Dec 2018 13:10 |
| Last Modified: | 17 Sep 2020 07:54 |
| URI: | https://pred.uni-regensburg.de/id/eprint/990 |
Actions (login required)
 |
View Item |
