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Treatment of Intracranial Hemorrhagic Lesions Associated With Jacobsen’s Syndrome
Jacobsen's syndrome is a rare genetic disorder caused by deletion of the long arm of chromosome 11 (11q) and is characterized primarily by craniofacial dysmorphism, congenital heart defects, intellectual disability, Paris-Treussaud hemorrhagic disorder, structural renal defects, and immunodefic...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Cureus
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499498/ https://www.ncbi.nlm.nih.gov/pubmed/37711911 http://dx.doi.org/10.7759/cureus.43486 |