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Turner Syndrome and Neurofibromatosis 1: Rare Co-Existence with Important Clinical Implications
A 16.5-year-old Indian female presented with secondary amenorrhoea, cubitus valgus, scoliosis and multiple lentigines on the face. Karyotyping revealed mosaic Turner syndrome (TS) with 45, X/46, X iXq. She also had multiple café-au-lait macules and axillary freckles but no neurofibroma and did not f...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Journal of the ASEAN Federation of Endocrine Societies
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213385/ https://www.ncbi.nlm.nih.gov/pubmed/37252421 http://dx.doi.org/10.15605/jafes.038.01.20 |