PREPL deficiency : Delineation of the phenotype and development of a functional blood assay
(2018) In Genetics in Medicine 20(1). p.109-118- Abstract
PurposePREPL deficiency causes neonatal hypotonia, ptosis, neonatal feeding difficulties, childhood obesity, xerostomia, and growth hormone deficiency. Different recessive contiguous gene deletion syndromes involving PREPL and a variable combination of SLC3A1 (hypotonia-cystinuria syndrome), CAMKMT (atypical hypotonia-cystinuria syndrome), and PPM1B (2p21 deletion syndrome) have been described. In isolated PREPL deficiency, previously described only once, the absence of cystinuria complicates the diagnosis. Therefore, we developed a PREPL blood assay and further delineated the phenotype.MethodsClinical features of new subjects with PREPL deficiency were recorded. The presence of PREPL in lymphocytes and its reactivity with an... (More)
PurposePREPL deficiency causes neonatal hypotonia, ptosis, neonatal feeding difficulties, childhood obesity, xerostomia, and growth hormone deficiency. Different recessive contiguous gene deletion syndromes involving PREPL and a variable combination of SLC3A1 (hypotonia-cystinuria syndrome), CAMKMT (atypical hypotonia-cystinuria syndrome), and PPM1B (2p21 deletion syndrome) have been described. In isolated PREPL deficiency, previously described only once, the absence of cystinuria complicates the diagnosis. Therefore, we developed a PREPL blood assay and further delineated the phenotype.MethodsClinical features of new subjects with PREPL deficiency were recorded. The presence of PREPL in lymphocytes and its reactivity with an activity-based probe were evaluated by western blot.ResultsFive subjects with isolated PREPL deficiency, three with hypotonia-cystinuria syndrome, and two with atypical hypotonia-cystinuria syndrome had nine novel alleles. Their IQs ranged from 64 to 112. Adult neuromuscular signs included ptosis, nasal dysarthria, facial weakness, and variable proximal and neck flexor weakness. Autonomic features are prevalent. PREPL protein and reactivity were absent in lymphocytes from subjects with PREPL deficiency, but normal in the clinically similar Prader-Willi syndrome.ConclusionPREPL deficiency causes neuromuscular, autonomic, cognitive, endocrine, and dysmorphic clinical features. PREPL is not deficient in Prader-Willi syndrome. The novel blood test should facilitate the confirmation of PREPL deficiency.
(Less)
- author
- organization
- publishing date
- 2018-01-01
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- blood assay, hypotonia-cystinuria syndrome, neonatal hypotonia8Prader-Willi syndrome, PREPL
- in
- Genetics in Medicine
- volume
- 20
- issue
- 1
- pages
- 10 pages
- publisher
- Nature Publishing Group
- external identifiers
-
- pmid:28726805
- pmid:28726805
- scopus:85040465071
- ISSN
- 1098-3600
- DOI
- 10.1038/gim.2017.74
- language
- English
- LU publication?
- yes
- id
- d89c9c9a-a02a-4229-8ec8-eaf587a364ed
- date added to LUP
- 2018-02-05 12:23:43
- date last changed
- 2024-03-01 13:34:49
@article{d89c9c9a-a02a-4229-8ec8-eaf587a364ed, abstract = {{<p>PurposePREPL deficiency causes neonatal hypotonia, ptosis, neonatal feeding difficulties, childhood obesity, xerostomia, and growth hormone deficiency. Different recessive contiguous gene deletion syndromes involving PREPL and a variable combination of SLC3A1 (hypotonia-cystinuria syndrome), CAMKMT (atypical hypotonia-cystinuria syndrome), and PPM1B (2p21 deletion syndrome) have been described. In isolated PREPL deficiency, previously described only once, the absence of cystinuria complicates the diagnosis. Therefore, we developed a PREPL blood assay and further delineated the phenotype.MethodsClinical features of new subjects with PREPL deficiency were recorded. The presence of PREPL in lymphocytes and its reactivity with an activity-based probe were evaluated by western blot.ResultsFive subjects with isolated PREPL deficiency, three with hypotonia-cystinuria syndrome, and two with atypical hypotonia-cystinuria syndrome had nine novel alleles. Their IQs ranged from 64 to 112. Adult neuromuscular signs included ptosis, nasal dysarthria, facial weakness, and variable proximal and neck flexor weakness. Autonomic features are prevalent. PREPL protein and reactivity were absent in lymphocytes from subjects with PREPL deficiency, but normal in the clinically similar Prader-Willi syndrome.ConclusionPREPL deficiency causes neuromuscular, autonomic, cognitive, endocrine, and dysmorphic clinical features. PREPL is not deficient in Prader-Willi syndrome. The novel blood test should facilitate the confirmation of PREPL deficiency.</p>}}, author = {{Régal, Luc and Mårtensson, Emma and Maystadt, Isabelle and Voermans, Nicol and Lederer, Damien and Burlina, Alberto and Juan Fita, María Jesús and Hoogeboom, A. Jeannette M. and Olsson Engman, Mia and Hollemans, Tess and Schouten, Meyke and Meulemans, Sandra and Jonson, Tord and François, Inge and Gil Ortega, David and Kamsteeg, Erik Jan and Creemers, John W.M.}}, issn = {{1098-3600}}, keywords = {{blood assay; hypotonia-cystinuria syndrome; neonatal hypotonia8Prader-Willi syndrome; PREPL}}, language = {{eng}}, month = {{01}}, number = {{1}}, pages = {{109--118}}, publisher = {{Nature Publishing Group}}, series = {{Genetics in Medicine}}, title = {{PREPL deficiency : Delineation of the phenotype and development of a functional blood assay}}, url = {{http://dx.doi.org/10.1038/gim.2017.74}}, doi = {{10.1038/gim.2017.74}}, volume = {{20}}, year = {{2018}}, }