Publications by authors named "Virginia Fano"

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Prevalence of low birth weight, short length, and body disproportion at birth in patients with skeletal dysplasias: A retrospective study.
Silvana S Chiaramonte, Mariana Del Pino, Virginia Fano

Arch Argent Pediatr· December 2025

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Spine surgery in a rare case of Mégarbané-Dagher-Melki type spondylometaphyseal dysplasia. A Case Report.
Sofía Frank, Lucas Piantoni, Ulises Caraballo Correa, Eduardo Galaretto, Rodrigo G Remondino, Virginia Fano

Eur Spine J· December 2025

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Burosumab Treatment in a Girl With Cutaneous Skeletal Hypophosphatemia Syndrome: 2-Year Follow-Up.
Mariana Del Pino, Gisela Viterbo, María Agustina Valentini, Roberto Salvatierra, Florencia Belleri, Virginia Fano

Am J Med Genet A· June 2025

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New Argentine head circumference references for people with achondroplasia from 0 to 21 years of age.
Mariana Del Pino, Virginia Fano

Arch Argent Pediatr· June 2025

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Unexpected findings in cervical spine in spondylometaphyseal dysplasia Sutcliff type FN1-related.
Rosario Ramos-Mejía, Karen E Heath, Silvia Modamio-Høybjør, Victoria Huckstadt, Julián Calcagni, Virginia Fano

Am J Med Genet A· March 2024

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Growth in puberty in girls with hypochondroplasia, p.Asn540Lys-related mutations.
Mariana Del Pino, Virginia Fano

Am J Med Genet A· February 2024

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Clinical and auxological characteristics and quality of life of 50 children and adolescents with segmental overgrowth syndromes at a single center.
María V Wolf, Angélica A Moresco, Virginia Fano, Silvia Caino

Arch Argent Pediatr· December 2023

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Lifetime Impact Study for Achondroplasia (LISA): Findings from an observational and multinational study focused on health-related quality of life in individuals with achondroplasia in Latin America.
Juan Llerena, Pablo Rosselli, Amanda Aragão, Cristina Valenzuela, Debora Bertola, Virginia Fano

Genet Med Open· November 2023

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Clinical and radiological heterogeneity for the rare FGFR3 variant, p.Ser344Cys, description of a third patient.
Mariana Del Pino, Victoria Huckstadt, Francisca Diaz-Gonzalez, Maria Gabriela Obregon, Karen E Heath, Virginia Fano

Am J Med Genet A· August 2023

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Acetabular Protrusion in a Cohort of Patients with Osteogenesis Imperfecta Evaluated in a Pediatric Hospital.
Rosario Ramos-Mejía, Francisco Monterroza-Quintana, Claudio Primomo, Rodolfo Goyeneche, Virginia Fano

J Pediatr Genet· March 2023

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Isolated lateralized overgrowth: clinical, radiological, and auxological characteristics of a single-site cohort of 76 cases.
María J Romaris, Silvia Caino, Paula Adamo, Virginia Fano

Arch Argent Pediatr· December 2022

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Clinical and Genetic Analysis of Multiple Osteochondromas in A Cohort of Argentine Patients.
Silvia Caino, Marisa Angelica Cubilla, Romina Alba, María Gabriela Obregón, Virginia Fano

Genes (Basel)· November 2022

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Achondroplasia in Latin America: practical recommendations for the multidisciplinary care of pediatric patients.
Juan Llerena, Chong Ae Kim, Virginia Fano, Pablo Rosselli, Paulo Ferrez Collett-Solberg

BMC Pediatr· August 2022

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Osteochondromatosis: clinical variability and factors related to quality of life in children and adults.
Silvia Caino, Romina Alba, Silvina Bevilacqua, Mariana Roizen, María G Obregón, Virginia Fano

Arch Argent Pediatr· June 2022

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International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia.
Ravi Savarirayan, Penny Ireland, Melita Irving, Dominic Thompson, Inês Alves, Virginia Fano

Nat Rev Endocrinol· March 2022

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Impact of achondroplasia on Latin American patients: a systematic review and meta-analysis of observational studies.
Virginia Fano, Chong A Kim, Pablo Rosselli, Regina El Dib, Renée Shediac

Orphanet J Rare Dis· January 2022

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Hereditary hypophosphatemic rickets and craniosynostosis.
María Alejandra Arenas, Sebastián Jaimovich, Natalia Perez Garrido, Mariana Del Pino, Gisela Viterbo, Virginia Fano

J Pediatr Endocrinol Metab· September 2021

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A few challenges in mucopolysaccharidosis type I.
Luisa Bay, Hernán Amartino, Alejandra Antacle, Claudia Arberas, Adriana Berretta, Virginia Fano

Arch Argent Pediatr· June 2021

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Lifetime impact of achondroplasia: Current evidence and perspectives on the natural history.
Julie Hoover-Fong, Moira S Cheung, Virginia Fano, Lars Hagenas, Jacqueline T Hecht

Bone· May 2021

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Description of four patients with TRIP11 variants expand the clinical spectrum of odontochondroplasia (ODCD) and demonstrate the existence of common variants.
Mariana Del Pino, Maria José Sanchez-Soler, Manuel Parrón-Pajares, Miriam Aza-Carmona, Karen E Heath, Virginia Fano

Eur J Med Genet· May 2021

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New recommendations for the care of patients with mucopolysaccharidosis type I.
Luisa Bay, Hernán Amartino, Alejandra Antacle, Claudia Arberas, Adriana Berretta, Virginia Fano

Arch Argent Pediatr· April 2021

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Delineation of the clinical and radiological features of Stuve-Wiedemann syndrome childhood survivors, four new cases and review of the literature.
Sofía M Siccha, Anna María Cueto, Manuel Parrón-Pajares, Gaspar González-Morán, Marta Pacio-Miguez, Virginia Fano

Am J Med Genet A· March 2021

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Growth in achondroplasia, from birth to adulthood, analysed by the JPA-2 model.
Mariana Del Pino, Virginia Fano, Paula Adamo

J Pediatr Endocrinol Metab· December 2020

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Skeletal dysplasias in Latin America.
Denise P Cavalcanti, Virginia Fano, Cecilia Mellado, Maria Dora J Lacarrubba-Flores, Cynthia Silveira

Am J Med Genet C Semin Med Genet· December 2020

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Clinical and Radiologic Evaluation of an Individual with Hypochondroplasia and a Novel FGFR3 Mutation.
Rosario Ramos Mejía, Miriam Aza-Carmona, Mariana Del Pino, Karen E Heath, Virginia Fano

J Pediatr Genet· March 2020

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