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Società Italiana Malattie Genetiche Pediatriche e Disabilità Congenite

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SIMGePeD

Società Italiana Malattie Genetiche Pediatriche e Disabilità Congenite

La cura del Bambino









Febbraio 28, 2025

Management of neurofibromatosis type 1-associated plexiform neurofibromas

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Febbraio 28, 2025

Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome

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Febbraio 28, 2025

Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

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Febbraio 28, 2025

European Academy of Andrology Guidelines on Klinefelter Syndrome

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Febbraio 28, 2025

Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendations

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Febbraio 28, 2025

A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome

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Febbraio 28, 2025

Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations

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Febbraio 28, 2025

Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement

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Febbraio 28, 2025

International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia

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Febbraio 28, 2025

Vademecum – per genitori a contatto con la disabilità

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Genereview
Rivista malattie rare
Orphanet
American Journal medical genetics part A
Sindrome di Treacher Collins (Sindrome di Franceschetti)
Systematic Review of Current Audiological Treatment Options for Patients with Treacher Collins Syndrome (2024)
Treacher Collins syndrome: A comprehensive review on clinical features, diagnosis, and management (2024)

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