MON-072 A 2 -Year Old Girl with Turner Syndrome and Neurofibromatosis Type 1

Introduction: Turner syndrome (TS) occurs due to loss of either all or part of the X chromosome, in some or all the cells of the body. The most consistent features of TS are short stature and premature ovarian failure. Neurofibromatosis type 1 (NF1) is an inheritable in an autosomal dominant manner...

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Detalles Bibliográficos
Autores principales: Dermitzaki, Eleni, Manolakos, Emmanouil, Tagalakis, Panagiotis, Kleanthous, Kleanthis, Papadimitriou, Dimitrios T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207529/
http://dx.doi.org/10.1210/jendso/bvaa046.1798

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207529/
http://dx.doi.org/10.1210/jendso/bvaa046.1798

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