Results 1 to 10 of about 3,407 (171)

A de novo start-loss variant in the NIPBL gene causing mild type 1 Cornelia de Lange syndrome in an Iranian family: A Case Report [PDF]

Journal of Medical Case Reports
Background Cornelia de Lange syndrome is a rare congenital disorder marked by considerable clinical variability, including intellectual disability, growth retardation, distinctive facial features, limb abnormalities, and multisystem involvement.
Atefeh Mir, Zahra Abbasi, Yongjun Song, Hane Lee, Ali Khajeh, Mojdeh Jahantigh, Samira Hajigholami, Shadi Khedri, Mohammad-Amin Tabatabaiefar   +8 more
doaj   +2 more sources

Audiological Characterization of Individuals with Cornelia de Lange Syndrome [PDF]

International Archives of Otorhinolaryngology
Introduction Cornelia de Lange Syndrome (CdLS) is a genetic disorder in which individuals may present sensorineural and/or conductive hearing loss, and the results of behavioral auditory assessments are not accurate.
Nayara Pereira Santos, Liliane Aparecida Fagundes Silva, Ivone Ferreira Neves-Lobo, Chong Ae Kim, Carla Gentile Matas   +4 more
doaj   +2 more sources

Neuropsychiatric manifestations in Cornelia de Lange syndrome [PDF]

European Psychiatry, 2023
Introduction Cornelia De Lange syndrome (CdLS) is a dominant and rare genetically heterogeneous syndrome. It is characterized by a large phenotypical spectrum going from a classical to a non-classical form affecting multiple organ systems including ...
F. Majdoub, A. Souissi, M. Trabelsi, A. Ziadi, N. Belguith, F. Maazoul, M. Guirat, I. Boujelbene, H. Kamoun, R. Mrad, S. Masmoudi, I. Ben Ayed   +11 more
doaj   +2 more sources

Neurobehavioral and developmental profiles: genotype–phenotype correlations in individuals with Cornelia de Lange syndrome [PDF]

Orphanet Journal of Rare Diseases
Background Cornelia de Lange (CdLS) is a rare genetic disorder that affects most body systems. Variants in multiple genes including NIPBL and SMC1A, can cause the syndrome.
Rowena Ng, Julia O’Connor, Deirdre Summa, Antonie D. Kline   +3 more
doaj   +2 more sources

The phenotypic spectrum of the Cornelia de Lange‐like “Alazami‐Yuan syndrome”: A case report of the 7th diagnosed individual and review of the literature [PDF]

Clinical Case Reports
Key Clinical Message We present a 17‐year‐old female with a childhood clinical diagnosis of Cornelia de Lange Syndrome (CdLS), however later genetic testing identified compound heterozygous variants in TAF6, consistent with AYS.
Annie Pappas, Mary Mooney, Katherine Kohnen, Joshua W. Owens, Wenying Zhang, Robert J. Hopkin, Amelle Shillington   +6 more
doaj   +2 more sources

Nasal polyposis in pediatric patients with Cornelia de Lange syndrome: endoscopic diagnosis, treatment and follow up in two case reports

Italian Journal of Pediatrics, 2023
Background Cornelia de Lange syndrome is a rare genetic disease with otolaryngological involvement. The classic phenotype is characterized by distinctive facial features, intellectual disability, growth delay, hirsutism, and upper-limb reduction.
Roberta Onesimo, Rita De Santis, Chiara Leoni, Mario Rigante, Marco Piastra, Elisabetta Sforza, Angelo Selicorni, Giuseppe Zampino   +7 more
doaj   +1 more source

Síndrome de Cornelia de Lange y su relación con la erupción dentaria. Análisis caso clínico.

Revista de Odontopediatria Latinoamericana, 2022
El Síndrome de Cornelia de Lange (SCDL), es una anomalía genética cuya prevalencia es de 1:62.000-1:45.000 de los nacimientos. Se atribuye principalmente a mutaciones en los genes NIPBL, SMC3 y SMC1A.
Lelimar Palencia Torres, Josnelly Santaella Pantoja, Ysabel Zamudio Acosta, Neorlay Rondón Jiménez   +3 more
doaj   +1 more source

Case study of girl with Cornelia de Lange syndrome

Listy klinicke logopedie, 2023
Cornelia de Lange Syndrome is a genetic syndrome with manifestations in the somatic, cognitive and perceptual areas. It is characterised by interindividual differences among patients with this diagnosis. Impairments include vision and hearing impairments,
Adelaida Fábianová, Žofia Frajková, Miroslav Tedla   +2 more
doaj   +1 more source

Disfagia orofaríngea em crianças com síndrome Cornélia De Lange: série de casos

Distúrbios da Comunicação, 2020
Introdução: A síndrome Cornélia De Lange (CdLS) é caracterizada por ser polimalformativa que envolve anomalias faciais, atraso de crescimento e desenvolvimento psicomotor, alterações comportamentais e malformações associadas.
Vanessa Souza Gigoski de Miranda, Andressa de Moura Barbosa, Lisiane de Rosa Barbosa, Gilberto Bueno Fischer, Rafaela Soares Rech   +4 more
doaj   +1 more source

Classic Cornelia de Lange syndrome with variant of unknown significance detected in NIPBL gene mutation: a case report

Egyptian Journal of Medical Human Genetics, 2021
Background Cornelia de Lange syndrome is a relatively uncommon disorder associated with multiple congenital anomalies/mental retardation of unknown etiology with its incidence varying from 1:10,000 to 1:50,000 live births in different population groups ...
Jay J. Desai, Sreelata B. Nair, S. Pappachan   +2 more
doaj   +1 more source