{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T06:09:40Z","timestamp":1761718180219},"reference-count":34,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2011,5,27]],"date-time":"2011-05-27T00:00:00Z","timestamp":1306454400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2011,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Zimmermann\u2013Laband syndrome (ZLS) is a rare disorder characterized by gingival fibromatosis, hypertrichosis, intellectual disability, and absence and\/or hypoplasia of the nails or terminal phalanges of the hands and feet. The syndromic features of ZLS are highly variable and can overlap with other entities featuring gingival fibrosis. This study describes a patient with ZLS with novel findings, including colpocephaly, hemivertebra, polydactyly, hyperpigmentation, and hemihyperplasia. Thus, the present report expands the phenotypic spectrum of this uncommon syndrome. \u00a9 2011 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.34030","type":"journal-article","created":{"date-parts":[[2011,5,27]],"date-time":"2011-05-27T17:39:54Z","timestamp":1306517994000},"page":"1716-1720","source":"Crossref","is-referenced-by-count":18,"title":["Expanding the phenotype of gingival fibromatosis\u2013mental retardation\u2013hypertrichosis (Zimmermann\u2013Laband) syndrome"],"prefix":"10.1002","volume":"155","author":[{"given":"Oscar F.","family":"Chacon\u2010Camacho","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Johanna","family":"V\u00e1zquez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Juan C.","family":"Zenteno","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2011,5,27]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.32034"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1097\/MCD.0b013e3282f2514c"},{"key":"e_1_2_4_4_1","first-page":"349","article-title":"Elephantiasis gingivae: Report of an affected family with associated hepatomegaly, soft tissue, and skeletal abnormalities","volume":"37","author":"Alavandar G","year":"1965","journal-title":"J All India Dent Assoc"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1469-8749.1989.tb04033.x"},{"key":"e_1_2_4_6_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1600-0714.1991.tb00438.x"},{"key":"e_1_2_4_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/0030-4220(94)90118-X"},{"key":"e_1_2_4_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/0278-2391(88)90229-7"},{"key":"e_1_2_4_9_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320310326"},{"key":"e_1_2_4_10_1","doi-asserted-by":"publisher","DOI":"10.1097\/MCD.0b013e32832dc393"},{"key":"e_1_2_4_11_1","doi-asserted-by":"publisher","DOI":"10.1902\/jop.1973.44.5.299"},{"key":"e_1_2_4_12_1","doi-asserted-by":"publisher","DOI":"10.1002\/1096-8628(20001127)95:3<241::AID-AJMG11>3.0.CO;2-N"},{"key":"e_1_2_4_13_1","doi-asserted-by":"crossref","first-page":"1093","DOI":"10.1093\/oso\/9780195118612.003.0026","volume-title":"Syndromes of the head and neck","author":"Gorlin RJ","year":"2001"},{"key":"e_1_2_4_14_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320220323"},{"key":"e_1_2_4_15_1","doi-asserted-by":"publisher","DOI":"10.1902\/jop.2003.74.8.1225"},{"key":"e_1_2_4_16_1","doi-asserted-by":"publisher","DOI":"10.1080\/01913120601042245"},{"key":"e_1_2_4_17_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1966.tb15231.x"},{"key":"e_1_2_4_18_1","first-page":"195","article-title":"Familial gingival fibromatosis associated with progressive deafness in five generations of a family","volume":"13","author":"Jones G","year":"1977","journal-title":"Birth Defects"},{"key":"e_1_2_4_19_1","first-page":"213","article-title":"Hereditary gingival fibromatosis and sensorineural hearing loss in a 42\u2010year\u2010old man with Jones syndrome","volume":"15","author":"Kasabo\u011flu O","year":"2004","journal-title":"Genet Counsel"},{"key":"e_1_2_4_20_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.31544"},{"key":"e_1_2_4_21_1","first-page":"459","article-title":"Gingival fibromatosis, mental retardation, epilepsy and hypertrichosis","volume":"32","author":"Kiss P","year":"1990","journal-title":"Dev Med Child Neurol"},{"key":"e_1_2_4_22_1","doi-asserted-by":"publisher","DOI":"10.1016\/0030-4220(64)90506-7"},{"key":"e_1_2_4_23_1","first-page":"251","article-title":"Congenital marked hypertrichosis and Laband syndrome in a child: Overlap between the gingival fibromatosis\u2010hypertrichosis and Lanband syndromes","volume":"5","author":"Lacombe D","year":"1994","journal-title":"Genet Couns"},{"key":"e_1_2_4_24_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ijom.2010.01.023"},{"key":"e_1_2_4_25_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320250305"},{"key":"e_1_2_4_26_1","doi-asserted-by":"publisher","DOI":"10.1016\/0030-4220(67)90416-1"},{"key":"e_1_2_4_27_1","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1096-8628(19980630)78:2<160::AID-AJMG12>3.0.CO;2-L"},{"key":"e_1_2_4_28_1","doi-asserted-by":"publisher","DOI":"10.1097\/00019605-199804000-00001"},{"key":"e_1_2_4_29_1","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.2.3678.9"},{"key":"e_1_2_4_30_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-263X.2004.00471.x"},{"key":"e_1_2_4_31_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(65)80413-9"},{"key":"e_1_2_4_32_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.10174"},{"key":"e_1_2_4_33_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1997.tb02432.x"},{"key":"e_1_2_4_34_1","doi-asserted-by":"publisher","DOI":"10.1902\/jop.1995.66.1.75"},{"key":"e_1_2_4_35_1","first-page":"419","article-title":"\u00dcber anomalien des (cases 1 and 2)","volume":"44","author":"Zimmermann KW","year":"1928","journal-title":"Vjschr Zahnheilkd"}],"container-title":["American Journal of Medical Genetics Part A"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.a.34030","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.a.34030","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,20]],"date-time":"2023-11-20T13:22:10Z","timestamp":1700486530000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.a.34030"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,5,27]]},"references-count":34,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2011,7]]}},"alternative-id":["10.1002\/ajmg.a.34030"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.a.34030","archive":["Portico"],"relation":{},"ISSN":["1552-4825","1552-4833"],"issn-type":[{"value":"1552-4825","type":"print"},{"value":"1552-4833","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,5,27]]}}}