Literature DB >> 25376364

Rare diseases in clinical endocrinology: a taxonomic classification system.

G Marcucci1, L Cianferotti2, P Beck-Peccoz3, M Capezzone4, F Cetani5, A Colao6, M V Davì7, E degli Uberti8, S Del Prato9, R Elisei5, A Faggiano6, D Ferone10, C Foresta11, L Fugazzola3, E Ghigo12, G Giacchetti13, F Giorgino14, A Lenzi15, P Malandrino16, M Mannelli17, C Marcocci18, L Masi19, F Pacini20, G Opocher21,22, A Radicioni23, M Tonacchera5, R Vigneri24, M C Zatelli8, M L Brandi25.   

Abstract

PURPOSE: Rare endocrine-metabolic diseases (REMD) represent an important area in the field of medicine and pharmacology. The rare diseases of interest to endocrinologists involve all fields of endocrinology, including rare diseases of the pituitary, thyroid and adrenal glands, paraganglia, ovary and testis, disorders of bone and mineral metabolism, energy and lipid metabolism, water metabolism, and syndromes with possible involvement of multiple endocrine glands, and neuroendocrine tumors. Taking advantage of the constitution of a study group on REMD within the Italian Society of Endocrinology, consisting of basic and clinical scientists, a document on the taxonomy of REMD has been produced. METHODS AND
RESULTS: This document has been designed to include mainly REMD manifesting or persisting into adulthood. The taxonomy of REMD of the adult comprises a total of 166 main disorders, 338 including all variants and subtypes, described into 11 tables.
CONCLUSIONS: This report provides a complete taxonomy to classify REMD of the adult. In the future, the creation of registries of rare endocrine diseases to collect data on cohorts of patients and the development of common and standardized diagnostic and therapeutic pathways for each rare endocrine disease is advisable. This will help planning and performing intervention studies in larger groups of patients to prove the efficacy, effectiveness, and safety of a specific treatment.

Entities:  

Keywords:  Endocrine glands; Endocrinopathy; Neuroendocrine tumors; Orphan disease; Taxonomy

Mesh:

Year:  2014        PMID: 25376364     DOI: 10.1007/s40618-014-0202-6

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  236 in total

1.  Pancreatic neuroendocrine neoplasms: diagnosis and management.

Authors:  Aparna Balachandran; Eric P Tamm; Priya R Bhosale; Madhavi Patnana; Raghu Vikram; Jason B Fleming; Matthew H Katz; Chuslip Charnsangavej
Journal:  Abdom Imaging       Date:  2013-04

2.  Epidemiology and natural history of Gaucher's disease.

Authors:  Atul Mehta
Journal:  Eur J Intern Med       Date:  2006-11       Impact factor: 4.487

3.  Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.

Authors:  Rossella Libé; Anelia Horvath; Delphine Vezzosi; Amato Fratticci; Joel Coste; Karine Perlemoine; Bruno Ragazzon; Marine Guillaud-Bataille; Lionel Groussin; Eric Clauser; Marie-Laure Raffin-Sanson; Jennifer Siegel; Jason Moran; Limor Drori-Herishanu; Fabio Rueda Faucz; Maya Lodish; Maria Nesterova; Xavier Bertagna; Jerome Bertherat; Constantine A Stratakis
Journal:  J Clin Endocrinol Metab       Date:  2010-11-03       Impact factor: 5.958

Review 4.  [Antenatal form of Bartter's syndrome].

Authors:  G Deschenes; A Burguet; C Guyot; P Hubert; M Garabedian; M Dechaux; C Loirat; M Broyer
Journal:  Ann Pediatr (Paris)       Date:  1993-02

5.  Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation.

Authors:  Peter M Krawitz; Yoshiko Murakami; Jochen Hecht; Ulrike Krüger; Susan E Holder; Geert R Mortier; Barbara Delle Chiaie; Elfride De Baere; Miles D Thompson; Tony Roscioli; Szymon Kielbasa; Taroh Kinoshita; Stefan Mundlos; Peter N Robinson; Denise Horn
Journal:  Am J Hum Genet       Date:  2012-06-07       Impact factor: 11.025

6.  K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension.

Authors:  Murim Choi; Ute I Scholl; Peng Yue; Peyman Björklund; Bixiao Zhao; Carol Nelson-Williams; Weizhen Ji; Yoonsang Cho; Aniruddh Patel; Clara J Men; Elias Lolis; Max V Wisgerhof; David S Geller; Shrikant Mane; Per Hellman; Gunnar Westin; Göran Åkerström; Wenhui Wang; Tobias Carling; Richard P Lifton
Journal:  Science       Date:  2011-02-11       Impact factor: 47.728

7.  Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure.

Authors:  C Fava; M Montagnana; L Rosberg; P Burri; P Almgren; A Jönsson; P Wanby; G Lippi; P Minuz; L U Hulthèn; M Aurell; O Melander
Journal:  Hum Mol Genet       Date:  2007-11-01       Impact factor: 6.150

Review 8.  Pituitary tumours: TSH-secreting adenomas.

Authors:  Paolo Beck-Peccoz; Luca Persani; Deborah Mannavola; Irene Campi
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2009-10       Impact factor: 4.690

9.  Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.

Authors:  M J Abramowicz; H M Targovnik; V Varela; P Cochaux; L Krawiec; M A Pisarev; F V Propato; G Juvenal; H A Chester; G Vassart
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

Review 10.  Enchondromatosis revisited: new classification with molecular basis.

Authors:  Andrea Superti-Furga; Jürgen Spranger; Gen Nishimura
Journal:  Am J Med Genet C Semin Med Genet       Date:  2012-07-12       Impact factor: 3.908

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  3 in total

1.  HABP2 G534E variation in familial non-medullary thyroid cancer: an Italian series.

Authors:  S Cantara; C Marzocchi; M G Castagna; F Pacini
Journal:  J Endocrinol Invest       Date:  2016-11-21       Impact factor: 4.256

Review 2.  Congenital Conditions of Hypophosphatemia Expressed in Adults.

Authors:  Gemma Marcucci; Maria Luisa Brandi
Journal:  Calcif Tissue Int       Date:  2020-05-14       Impact factor: 4.333

3.  The molecular classification of hereditary endocrine diseases.

Authors:  Lei Ye; Guang Ning
Journal:  Endocrine       Date:  2015-07-07       Impact factor: 3.633

  3 in total

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