Co-occurrence of neurofibromatosis type 1 and pseudoachondroplasia – a first case report

BACKGROUND: Neurofibromatosis type 1 and pseudoachondroplasia are both rare autosomal dominant disorders, caused by pathogenic mutations in NF1 and COMP genes, respectively. Both neurofibromin 1 and cartilage oligomeric matrix protein (COMP) play a role in the development of the skeleton. Carrying b...

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Detalles Bibliográficos
Autores principales: Pálla, Sára, Anker, Pálma, Farkas, Klára, Plázár, Dóra, Kiss, Sándor, Marschalkó, Péter, Szalai, Zsuzsanna, Bene, Judit, Hadzsiev, Kinga, Maróti, Zoltán, Kalmár, Tibor, Medvecz, Márta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993747/
https://www.ncbi.nlm.nih.gov/pubmed/36890482
http://dx.doi.org/10.1186/s12887-023-03920-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993747/
https://www.ncbi.nlm.nih.gov/pubmed/36890482
http://dx.doi.org/10.1186/s12887-023-03920-7

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