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Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C
dc.rights.license | open | en_US |
dc.contributor.author | PELLETIER, Felixe | |
dc.contributor.author | PERRIER, Stefanie | |
dc.contributor.author | CAYAMI, Ferdy K. | |
dc.contributor.author | MIRCHI, Amytice | |
dc.contributor.author | SAIKALI, Stephan | |
dc.contributor.author | TRAN, Luan T. | |
dc.contributor.author | ULRICK, Nicole | |
dc.contributor.author | GUERRERO, Kether | |
dc.contributor.author | RAMPAKAKIS, Emmanouil | |
dc.contributor.author | VAN SPAENDONK, Rosalina M. L. | |
dc.contributor.author | NAIDU, Sakkuba | |
dc.contributor.author | POHL, Daniela | |
dc.contributor.author | GIBSON, William T. | |
dc.contributor.author | DEMOS, Michelle | |
hal.structure.identifier | Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM] | |
dc.contributor.author | GOIZET, Cyril | |
dc.contributor.author | TEJERA-MARTIN, Ingrid | |
dc.contributor.author | POTIC, Ana | |
dc.contributor.author | FOGEL, Brent L. | |
dc.contributor.author | BRAIS, Bernard | |
dc.contributor.author | SYLVAIN, Michel | |
dc.contributor.author | SEBIRE, Guillaume | |
dc.contributor.author | LOURENCO, Charles Marques | |
dc.contributor.author | BONKOWSKY, Joshua L. | |
dc.contributor.author | CATSMAN-BERREVOETS, Coriene | |
dc.contributor.author | PINTO, Pedro S. | |
dc.contributor.author | TIRUPATHI, Sandya | |
dc.contributor.author | STROMME, Peter | |
dc.contributor.author | DE GRAUW, Ton | |
dc.contributor.author | GIERUSZCZAK-BIALEK, Dorota | |
dc.contributor.author | KRAGELOH-MANN, Ingeborg | |
dc.contributor.author | MIERZEWSKA, Hanna | |
dc.contributor.author | PHILIPPI, Heike | |
dc.contributor.author | RANKIN, Julia | |
dc.contributor.author | ATIK, Tahir | |
dc.contributor.author | BANWELL, Brenda | |
dc.contributor.author | BENKO, William S. | |
dc.contributor.author | BLASCHEK, Astrid | |
dc.contributor.author | BLEY, Annette | |
dc.contributor.author | BOLTSHAUSER, Eugen | |
dc.contributor.author | BRATKOVIC, Drago | |
dc.contributor.author | BROZOVA, Klara | |
dc.contributor.author | CIMAS, Iciar | |
dc.contributor.author | CLOUGH, Christopher | |
dc.contributor.author | CORENBLUM, Bernard | |
dc.contributor.author | DINOPOULOS, Argirios | |
dc.contributor.author | DOLAN, Gail | |
dc.contributor.author | FALETRA, Flavio | |
dc.contributor.author | FERNANDEZ, Raymond | |
dc.contributor.author | FLETCHER, Janice | |
dc.contributor.author | GARCIA GARCIA, Maria Eugenia | |
dc.contributor.author | GASPARINI, Paolo | |
dc.contributor.author | GBUREK-AUGUSTAT, Janina | |
dc.contributor.author | GONZALEZ, Moron, Dolores | |
dc.contributor.author | HAMATI, Aline | |
dc.contributor.author | HARTING, Inga | |
dc.contributor.author | HERTZBERG, Christophe | |
dc.contributor.author | HILL, Alan | |
dc.contributor.author | HOBSON, Grace M. | |
dc.contributor.author | INNES, A. Micheil | |
dc.contributor.author | KAUFFMAN, Marcelo | |
dc.contributor.author | KIRWIN, Susan M. | |
dc.contributor.author | KLUGER, Gerhard | |
dc.contributor.author | KOLDITZ, Petra | |
dc.contributor.author | KOTZAERIDOU, Urania | |
dc.contributor.author | LA PIANA, Roberta | |
dc.contributor.author | LISTON, Eriskay | |
dc.contributor.author | MCCLINTOCK, William | |
dc.contributor.author | MCENTAGART, Meriel | |
dc.contributor.author | MCKENZIE, Fiona | |
dc.contributor.author | MELANCON, Serge | |
dc.contributor.author | MISBAHUDDIN, Anjum | |
dc.contributor.author | SURI, Mohnish | |
dc.contributor.author | MONTON, Fernando I. | |
dc.contributor.author | MOUTTON, Sebastien | |
dc.contributor.author | MURPHY, Raymond P. J. | |
dc.contributor.author | NICKEL, Miriam | |
dc.contributor.author | ONAY, Huseyin | |
dc.contributor.author | ORCESI, Simona | |
dc.contributor.author | OZKLNAY, Ferda | |
dc.contributor.author | PATZER, Steffi | |
dc.contributor.author | PEDRO, Helio | |
dc.contributor.author | PEKIC, Sandra | |
dc.contributor.author | PINEDA MARFA, Mercedes | |
dc.contributor.author | PIZZINO, Amy | |
dc.contributor.author | PLECKO, Barbara | |
dc.contributor.author | POLL-THE, Bwee Tien | |
dc.contributor.author | POPOVIC, Vera | |
dc.contributor.author | RATING, Dietz | |
dc.contributor.author | RIOUX, Marie-France | |
dc.contributor.author | RODRIGUEZ ESPINOSA, Norberto | |
dc.contributor.author | RONAN, Anne | |
dc.contributor.author | OSTERGAARD, John R. | |
dc.contributor.author | ROSSIGNOL, Elsa | |
dc.contributor.author | SANCHEZ-CARPINTERO, Rocio | |
dc.contributor.author | SCHOSSIG, Anna | |
dc.contributor.author | SENBIL, Nesrin | |
dc.contributor.author | SONDERBERG ROOS, Laura K. | |
dc.contributor.author | STEVENS, Cathy A. | |
dc.contributor.author | SYNOFZIK, Matthis | |
dc.contributor.author | SZTRIHA, Laszlo | |
dc.contributor.author | TIBUSSEK, Daniel | |
dc.contributor.author | TIMMANN, Dagmar | |
dc.contributor.author | TONDUTI, Davide | |
dc.contributor.author | VAN DE WARRENBURG, Bart P. | |
dc.contributor.author | VAZQUEZ-LOPEZ, Maria | |
dc.contributor.author | VENKATESWARAN, Sunita | |
dc.contributor.author | WASLING, Pontus | |
dc.contributor.author | WASSMER, Evangeline | |
dc.contributor.author | WEBSTER, Richard I. | |
dc.contributor.author | WIEGAND, Gert | |
dc.contributor.author | YOON, Grace | |
dc.contributor.author | ROTTEVEEL, Joost | |
dc.contributor.author | SCHIFFMANN, Raphael | |
dc.contributor.author | VAN DER KNAAP, Marjo S. | |
dc.contributor.author | VANDERVER, Adeline | |
dc.contributor.author | MARTOS-MORENO, Gabriel A. | |
dc.contributor.author | POLYCHRONAKOS, Constantin | |
dc.contributor.author | WOLF, Nicole I. | |
dc.contributor.author | BERNARD, Genevieve | |
dc.date.accessioned | 2021-10-26T15:10:53Z | |
dc.date.available | 2021-10-26T15:10:53Z | |
dc.date.issued | 2021-10-01 | |
dc.identifier.issn | 0021-972X (print) 1945-7197 (online) | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/117084 | |
dc.description.abstractEn | Context: 4H or POLR3-related leukodystrophy is an autosomal recessive disorder typically characterized by hypomyelination, hypodontia, and hypogonadotropic hypogonadism, caused by biallelic pathogenic variants in POLR3A, POLR3B, POLR1C, and POLR3K. The endocrine and growth abnormalities associated with this disorder have not been thoroughly investigated to date. Objective: To systematically characterize endocrine abnormalities of patients with 4H leukodystrophy. Design: An international cross-sectional study was performed on 150 patients with genetically confirmed 4H leukodystrophy between 2015 and 2016. Endocrine and growth abnormalities were evaluated, and neurological and other non-neurological features were reviewed. Potential genotype/phenotype associations were also investigated. Setting: This was a multicenter retrospective study using information collected from 3 predominant centers. Patients: A total of 150 patients with 4H leukodystrophy and pathogenic variants in POLR3A, POLR3B, or POLR1C were included. Main Outcome Measures: Variables used to evaluate endocrine and growth abnormalities included pubertal history, hormone levels (estradiol, testosterone, stimulated LH and FSH, stimulated GH, IGF-I, prolactin, ACTH, cortisol, TSH, and T4), and height and head circumference charts. Results: The most common endocrine abnormalities were delayed puberty (57/74; 77% overall, 64% in males, 89% in females) and short stature (57/93; 61%), when evaluated according to physician assessment. Abnormal thyroid function was reported in 22% (13/59) of patients. Conclusions: Our results confirm pubertal abnormalities and short stature are the most common endocrine features seen in 4H leukodystrophy. However, we noted that endocrine abnormalities are typically underinvestigated in this patient population. A prospective study is required to formulate evidence-based recommendations for management of the endocrine manifestations of this disorder. | |
dc.language.iso | EN | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
dc.subject.en | 4H leukodystrophy | |
dc.subject.en | Hypogonadotropic hypogonadism | |
dc.subject.en | Hypomyelination | |
dc.subject.en | POLR3-related leukodystrophy | |
dc.title.en | Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C | |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1210/clinem/dgaa700 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Médecine humaine et pathologie | en_US |
dc.identifier.pubmed | 33005949 | en_US |
bordeaux.journal | Journal of Clinical Endocrinology and Metabolism | en_US |
bordeaux.page | E660-E674 | en_US |
bordeaux.volume | 106 | en_US |
bordeaux.hal.laboratories | Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 | en_US |
bordeaux.issue | 2 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | INSERM | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
bordeaux.identifier.funderID | Canadian Institutes of Health Research | en_US |
bordeaux.identifier.funderID | Fonds de recherche du Québec | en_US |
bordeaux.identifier.funderID | Fonds de Recherche du Québec - Santé | en_US |
hal.identifier | hal-03404588 | |
hal.version | 1 | |
hal.date.transferred | 2021-10-26T15:11:12Z | |
hal.export | true | |
dc.rights.cc | Pas de Licence CC | en_US |
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