Diagnostic and therapeutic approach of tall stature

dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorALBUQUERQUE, Edoarda V. A.
dc.contributor.authorSCALCO, Renata C.
dc.contributor.authorJORGE, Alexander A. L.
dc.date.accessioned2017-08-17T19:14:48Z
dc.date.available2017-08-17T19:14:48Z
dc.date.issued2017
dc.description.abstractTall stature is defined as a height of more than 2 standard deviations (s.d.) above average for same sex and age. Tall individuals are usually referred to endocrinologists so that hormonal disorders leading to abnormal growth are excluded. However, the majority of these patients have familial tall stature or constitutional advance of growth (generally associated with obesity), both of which are diagnoses of exclusion. It is necessary to have familiarity with a large number of rarer overgrowth syndromes, especially because some of them may have severe complications such as aortic aneurysm, thromboembolism and tumor predisposition and demand-specific follow-up approaches. Additionally, endocrine disorders associated with tall stature have specific treatments and for this reason their recognition is mandatory. With this review, we intend to provide an up-to-date summary of the genetic conditions associated with overgrowth to emphasize a practical diagnostic approach of patients with tall stature and to discuss the limitations of current growth interruption treatment options.
dc.description.indexMEDLINE
dc.description.sponsorshipSao Paulo Research Foundation (FAPESP) [2013/03236-5, 2016/03318-0]
dc.description.sponsorshipNational Council for Scientific and Technological Development (CNPq) [301871/2016-7]
dc.identifier.citationEUROPEAN JOURNAL OF ENDOCRINOLOGY, v.176, n.6, p.R339-R353, 2017
dc.identifier.doi10.1530/EJE-16-1054
dc.identifier.eissn1479-683X
dc.identifier.issn0804-4643
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/21219
dc.language.isoeng
dc.publisherBIOSCIENTIFICA LTD
dc.relation.ispartofEuropean Journal of Endocrinology
dc.rightsrestrictedAccess
dc.rights.holderCopyright BIOSCIENTIFICA LTD
dc.subject.otherbeckwith-wiedemann-syndrome
dc.subject.otherfragile-x-syndrome
dc.subject.otherpremature epiphyseal closure
dc.subject.otherestrogen-receptor-alpha
dc.subject.othersilver-russell-syndrome
dc.subject.othersex steroid treatment
dc.subject.otherof-the-literature
dc.subject.otherfinal height
dc.subject.othermarfan-syndrome
dc.subject.otheraromatase deficiency
dc.subject.wosEndocrinology & Metabolism
dc.titleDiagnostic and therapeutic approach of tall stature
dc.typearticle
dc.type.categoryreview
dc.type.versionpublishedVersion
dspace.entity.typePublication
hcfmusp.citation.scopus34
hcfmusp.contributor.author-fmusphcEDOARDA VASCO DE ALBUQUERQUE ALBUQUERQUE
hcfmusp.contributor.author-fmusphcRENATA DA CUNHA SCALCO
hcfmusp.contributor.author-fmusphcALEXANDER AUGUSTO DE LIMA JORGE
hcfmusp.description.beginpageR339
hcfmusp.description.endpageR353
hcfmusp.description.issue6
hcfmusp.description.volume176
hcfmusp.origemWOS
hcfmusp.origem.pubmed28274950
hcfmusp.origem.scopus2-s2.0-85021308663
hcfmusp.origem.wosWOS:000402481100006
hcfmusp.publisher.cityBRISTOL
hcfmusp.publisher.countryENGLAND
hcfmusp.relation.referenceBaron J, 2015, NAT REV ENDOCRINOL, V11, P735, DOI 10.1038/nrendo.2015.165
hcfmusp.relation.referenceBARTSCH O, 1988, EUR J PEDIATR, V147, P59, DOI 10.1007/BF00442613
hcfmusp.relation.referenceBenyi E, 2010, INT J PEDIAT ENDOCRI, V2010, DOI 10.1186/1687-9856-2010-740629
hcfmusp.relation.referenceBerdasco M, 2013, HUM GENET, V132, P359, DOI 10.1007/s00439-013-1271-x
hcfmusp.relation.referenceBinder G, 1997, EUR J PEDIATR, V156, P905, DOI 10.1007/s004310050740
hcfmusp.relation.referenceBocciardi R, 2007, HUM MUTAT, V28, P724, DOI 10.1002/humu.20511
hcfmusp.relation.referenceBoehm U, 2015, NAT REV ENDOCRINOL, V11, P547, DOI 10.1038/nrendo.2015.112
hcfmusp.relation.referenceBonfig W, 2017, CURR OPIN ENDOCRINOL, V24, P39, DOI 10.1097/MED.0000000000000308
hcfmusp.relation.referenceBUCKLER JMH, 1986, ARCH DIS CHILD, V61, P464
hcfmusp.relation.referenceBulun SE, 2014, FERTIL STERIL, V101, P323, DOI 10.1016/j.fertnstert.2013.12.022
hcfmusp.relation.referenceBUTLER MG, 1992, PEDIATRICS, V89, P1059
hcfmusp.relation.referenceButte NF, 2007, J NUTR, V137, P153
hcfmusp.relation.referenceCarel JC, 2009, HORM RES, V71, P228, DOI 10.1159/000201112
hcfmusp.relation.referenceChagin AS, 2007, BONE, V40, P1415, DOI 10.1016/j.bone.2006.12.066
hcfmusp.relation.referenceCousminer DL, 2013, HUM MOL GENET, V22, P2735, DOI 10.1093/hmg/ddt104
hcfmusp.relation.referencede Bruin C, 2015, NAT REV ENDOCRINOL, V11, P455, DOI 10.1038/nrendo.2015.72
hcfmusp.relation.referenceDecker R, 2002, J CLIN ENDOCR METAB, V87, P1634, DOI 10.1210/jc.87.4.1634
hcfmusp.relation.referencedeWaal WJ, 1996, J CLIN ENDOCR METAB, V81, P1206, DOI 10.1210/jc.81.3.1206
hcfmusp.relation.referenceDEWAAL WJ, 1995, ARCH DIS CHILD, V73, P311
hcfmusp.relation.referenceDEWAAL WJ, 1995, CLIN ENDOCRINOL, V43, P87
hcfmusp.relation.referenceDICKERMAN Z, 1984, ACTA PAEDIATR SCAND, V73, P530, DOI 10.1111/j.1651-2227.1984.tb09966.x
hcfmusp.relation.referenceDiGiovanna JJ, 2001, J AM ACAD DERMATOL, V45, pS176, DOI 10.1067/mjd.2001.113721
hcfmusp.relation.referenceDrop SLS, 1998, ENDOCR REV, V19, P540, DOI 10.1210/er.19.5.540
hcfmusp.relation.referenceEggermann K, 2016, EUR J HUM GENET, V24, P1377, DOI 10.1038/ejhg.2016.45
hcfmusp.relation.referenceEggermann T, 2008, TRENDS GENET, V24, P195, DOI 10.1016/j.tig.2008.01.003
hcfmusp.relation.referenceErkula G, 2002, AM J MED GENET, V109, P100, DOI 10.1002/ajmg.10312
hcfmusp.relation.referenceFennoy I., 2013, OPINION ENDOCRINOLOG, V20, P44, DOI [10.1097/MED.0b013e32835b7f15, DOI 10.1097/MED.0B013E32835B7F15]
hcfmusp.relation.referenceGarrone S, 2002, J CLIN ENDOCR METAB, V87, P5455, DOI 10.1210/jc.2002-020614
hcfmusp.relation.referenceGroth KA, 2013, J CLIN ENDOCR METAB, V98, P20, DOI 10.1210/jc.2012-2382
hcfmusp.relation.referenceGRUTERS A, 1989, EUR J PEDIATR, V149, P11, DOI 10.1007/BF02024324
hcfmusp.relation.referenceHannema SE, 2013, J CLIN ENDOCR METAB, V98, pE1988, DOI [10.1210/jc.2013-2358, 10.1210/jc.20130358]
hcfmusp.relation.referenceHendriks AEJ, 2012, J CLIN ENDOCR METAB, V97, P3107, DOI 10.1210/jc.2012-1078
hcfmusp.relation.referenceHendriks AEJ, 2011, J CLIN ENDOCR METAB, V96, P1098, DOI 10.1210/jc.2010-2244
hcfmusp.relation.referenceHendriks AEJ, 2010, J CLIN ENDOCR METAB, V95, P5233, DOI 10.1210/jc.2010-0435
hcfmusp.relation.referenceHermanussen M, 2010, HORM RES PAEDIAT, V74, P153, DOI 10.1159/000317440
hcfmusp.relation.referenceHINDMARSH PC, 1988, CLIN ENDOCRINOL, V29, P289, DOI 10.1111/j.1365-2265.1988.tb01227.x
hcfmusp.relation.referenceIravani M, 2017, J ENDOCRINOL, V232, P403, DOI 10.1530/JOE-16-0263
hcfmusp.relation.referenceJaruratanasirikul Somchit, 2006, Journal of the Medical Association of Thailand, V89, P1396
hcfmusp.relation.referenceJee YH, 2016, J PEDIATR-US, V173, P32, DOI 10.1016/j.jpeds.2016.02.068
hcfmusp.relation.referenceJohnson W, 2012, INT J OBESITY, V36, P535, DOI 10.1038/ijo.2011.238
hcfmusp.relation.referenceJOSS EE, 1992, ARCH DIS CHILD, V67, P1357
hcfmusp.relation.referenceJOSS EE, 1994, EUR J PEDIATR, V153, P797
hcfmusp.relation.referenceKant SG, 2007, EUR J MED GENET, V50, P1, DOI 10.1016/j.ejmg.2006.03.005
hcfmusp.relation.referenceKatsanis SH, 2013, NAT REV GENET, V14, P415, DOI 10.1038/nrg3493
hcfmusp.relation.referenceKatznelson L, 2014, J CLIN ENDOCR METAB, V99, P3933, DOI 10.1210/jc.2014-2700
hcfmusp.relation.referenceKeppler-Noreuil KM, 2015, AM J MED GENET A, V167, P287, DOI 10.1002/ajmg.a.36836
hcfmusp.relation.referenceKidd SA, 2014, PEDIATRICS, V134, P995, DOI 10.1542/peds.2013-4301
hcfmusp.relation.referenceKurotaki N, 2001, GENE, V279, P197, DOI 10.1016/S0378-1119(01)00750-8
hcfmusp.relation.referenceKwun Y, 2015, J KOREAN MED SCI, V30, P911, DOI 10.3346/jkms.2015.30.7.911
hcfmusp.relation.referenceLatronico AC, 2016, LANCET DIABETES ENDO, V4, P265, DOI 10.1016/S2213-8587(15)00380-0
hcfmusp.relation.referenceLee JM, 2006, ARCH PEDIAT ADOL MED, V160, P1035, DOI 10.1001/archpedi.160.10.1035
hcfmusp.relation.referenceLemcke B, 1996, J CLIN ENDOCR METAB, V81, P296, DOI 10.1210/jc.81.1.296
hcfmusp.relation.referenceLim D, 2009, HUM REPROD, V24, P741, DOI 10.1093/humrep/den406
hcfmusp.relation.referenceLiu F, 2014, HUM GENET, V133, P587, DOI 10.1007/s00439-013-1394-0
hcfmusp.relation.referenceLOESCH DZ, 1995, AM J MED GENET, V58, P249, DOI 10.1002/ajmg.1320580311
hcfmusp.relation.referenceLoeys BL, 2010, J MED GENET, V47, P476, DOI 10.1136/jmg.2009.072785
hcfmusp.relation.referenceLouhiala P, 2009, J MED ETHICS, V35, P713, DOI 10.1136/jme.2009.030189
hcfmusp.relation.referenceLozano R, 2016, INTRACTABLE RARE DIS, V5, P145, DOI 10.5582/irdr.2016.01048
hcfmusp.relation.referenceLuscan A, 2014, J MED GENET, V51, P512, DOI 10.1136/jmedgenet-2014-102402
hcfmusp.relation.referenceMarchini A, 2016, ENDOCR REV, V37, P417, DOI 10.1210/er.2016-1036
hcfmusp.relation.referenceMiedlich SU, 2016, BONE, V93, P181, DOI 10.1016/j.bone.2016.09.024
hcfmusp.relation.referenceMiller DT, 2010, AM J HUM GENET, V86, P749, DOI 10.1016/j.ajhg.2010.04.006
hcfmusp.relation.referenceMORISHIMA A, 1995, J CLIN ENDOCR METAB, V80, P3689, DOI 10.1210/jc.80.12.3689
hcfmusp.relation.referenceNilsson O, 2005, HORM RES, V64, P157, DOI 10.1159/000088791
hcfmusp.relation.referenceNilsson O, 2003, ENDOCRINOLOGY, V144, P1481, DOI 10.1210/en.2002-221108
hcfmusp.relation.referenceNishimura G, 1997, EUR J PEDIATR, V156, P432, DOI 10.1007/s004310050631
hcfmusp.relation.referenceNoordam C, 2006, EUR J ENDOCRINOL, V154, P253, DOI 10.1530/eje.1.02087
hcfmusp.relation.referenceNORMANN EK, 1991, ARCH DIS CHILD, V66, P1275
hcfmusp.relation.referenceNoyes JJ, 2016, HORM RES PAEDIAT, V85, P69, DOI 10.1159/000441140
hcfmusp.relation.referenceOdink RJ, 2006, EUR J PEDIATR, V165, P50, DOI 10.1007/s00431-005-1722-z
hcfmusp.relation.referenceOtter M, 2010, EUR J HUM GENET, V18, P265, DOI 10.1038/ejhg.2009.109
hcfmusp.relation.referenceOttesen AM, 2010, AM J MED GENET A, V152A, P1206, DOI 10.1002/ajmg.a.33334
hcfmusp.relation.referenceOunap K, 2016, MOL SYNDROMOL, V7, P110, DOI 10.1159/000447413
hcfmusp.relation.referencePapadimitriou A, 2010, J CLIN ENDOCR METAB, V95, P4535, DOI 10.1210/jc.2010-0895
hcfmusp.relation.referencePicker JD, 1993, GENEREVIEWS R
hcfmusp.relation.referencePRENDIVILLE J, 1986, J AM ACAD DERMATOL, V15, P1259, DOI 10.1016/S0190-9622(86)70300-9
hcfmusp.relation.referencePyett P, 2005, SOC SCI MED, V61, P1629, DOI 10.1016/j.socsimed.2005.03.016
hcfmusp.relation.referenceRadivojevic U, 2006, CLIN ENDOCRINOL, V64, P423, DOI 10.1111/j.1365-2265.2006.02485.x
hcfmusp.relation.referenceRask O, 2008, ACTA PAEDIATR, V97, P342, DOI 10.1111/j.1651-2227.2007.00635.x
hcfmusp.relation.referenceRochira V, 2009, NAT REV ENDOCRINOL, V5, P559, DOI 10.1038/nrendo.2009.176
hcfmusp.relation.referenceRostomyan L, 2015, ENDOCR-RELAT CANCER, V22, P745, DOI 10.1530/ERC-15-0320
hcfmusp.relation.referenceSakai LY, 2016, GENE, V591, P279, DOI 10.1016/j.gene.2016.07.033
hcfmusp.relation.referenceSaul RA, 1993, GENEREVIEWS R
hcfmusp.relation.referenceSchafgen J, 2016, EUR J HUM GENET, V24, P1739, DOI 10.1038/ejhg.2016.90
hcfmusp.relation.referenceSCHOENLE EJ, 1987, J CLIN ENDOCR METAB, V65, P355
hcfmusp.relation.referenceShuman C, 1993, GENEREVIEWS R
hcfmusp.relation.referenceStalman SE, 2015, J CLIN RES PEDIATR E, V7, P260, DOI 10.4274/jcrpe.2220
hcfmusp.relation.referenceStovitz SD, 2011, AM J HUM BIOL, V23, P635, DOI 10.1002/ajhb.21191
hcfmusp.relation.referenceTarailo-Graovac M, 2016, NEW ENGL J MED, V374, P2246, DOI 10.1056/NEJMoa1515792
hcfmusp.relation.referenceTartaglia NR, 2010, ORPHANET J RARE DIS, V5, DOI 10.1186/1750-1172-5-8
hcfmusp.relation.referenceTatton-Brown K, 2005, AM J HUM GENET, V77, P193, DOI 10.1086/432082
hcfmusp.relation.referenceTatton-Brown K, 2007, EUR J HUM GENET, V15, P264, DOI 10.1038/sj.ejhg.5201686
hcfmusp.relation.referenceThauvin-Robinet C, 2016, CLIN GENET, V89, pE1, DOI 10.1111/cge.12704
hcfmusp.relation.referenceThomsett MJ, 2009, J PAEDIATR CHILD H, V45, P58, DOI 10.1111/j.1440-1754.2008.01428.x
hcfmusp.relation.referenceUpners EN, 2016, PEDIATR RES, V80, P693, DOI 10.1038/pr.2016.128
hcfmusp.relation.referenceVasques GA, 2014, HORM RES PAEDIAT, V82, P222, DOI 10.1159/000365049
hcfmusp.relation.referenceVenn A, 2004, LANCET, V364, P1513, DOI 10.1016/S0140-6736(04)17274-7
hcfmusp.relation.referenceVenn A, 2008, CLIN ENDOCRINOL, V68, P926, DOI 10.1111/j.1365-2265.2007.03128.x
hcfmusp.relation.referenceVidal O, 2000, P NATL ACAD SCI USA, V97, P5474, DOI 10.1073/pnas.97.10.5474
hcfmusp.relation.referenceVilar L, 2017, PITUITARY, V20, P22, DOI 10.1007/s11102-016-0772-8
hcfmusp.relation.referenceWeimann E, 1998, ARCH DIS CHILD, V78, P148
hcfmusp.relation.referenceWENG EY, 1995, AM J MED GENET, V56, P366, DOI 10.1002/ajmg.1320560405
hcfmusp.relation.referenceWigby K, 2016, AM J MED GENET A, V170, P2870, DOI 10.1002/ajmg.a.37688
hcfmusp.relation.referenceWikstrom AM, 2011, BEST PRACT RES CL EN, V25, P239, DOI 10.1016/j.beem.2010.09.006
hcfmusp.relation.referenceWong GWK, 1999, EUR J PEDIATR, V158, P776, DOI 10.1007/s004310051202
hcfmusp.relation.referenceWood AR, 2014, NAT GENET, V46, P1173, DOI 10.1038/ng.3097
hcfmusp.relation.referenceWright CM, 1999, ARCH DIS CHILD, V81, P257
hcfmusp.relation.referenceYang YP, 2014, JAMA-J AM MED ASSOC, V312, P1870, DOI 10.1001/jama.2014.14601
hcfmusp.scopus.lastupdate2024-05-10
relation.isAuthorOfPublication4fb59f7a-44f1-4329-9d4e-eb2963abe0a2
relation.isAuthorOfPublication56879ba1-07fd-46f2-b7de-551540906466
relation.isAuthorOfPublication872493f0-3232-484e-a574-207e16fcf202
relation.isAuthorOfPublication.latestForDiscovery4fb59f7a-44f1-4329-9d4e-eb2963abe0a2
Arquivos
Pacote Original
Agora exibindo 1 - 1 de 1
Nenhuma Miniatura disponível
Nome:
art_ALBUQUERQUE_Diagnostic_and_therapeutic_approach_of_tall_stature_2017.PDF
Tamanho:
2.01 MB
Formato:
Adobe Portable Document Format
Descrição:
publishedVersion (English)