Alfei Enrico, Cattaneo Elisa, Spaccini Luigina, Iascone Maria, Veggiotti Pierangelo, Doneda Chiara
Pediatric Neurology Unit, Department of Pediatrics, "Vittore Buzzi" Children's Hospital - ASST Fatebenefratelli-Sacco, Milan, Italy.
Clinical Genetics Unit, Department of Pediatrics, "Vittore Buzzi" Children's Hospital - ASST Fatebenefratelli-Sacco, Milan, Italy.
Neuropediatrics. 2022 Aug;53(4):283-286. doi: 10.1055/s-0041-1736193. Epub 2021 Nov 29.
We report a patient affected by -related disorder, providing the first extensive demonstration of clinical and neuroradiological progressive course of the disease, with possible implications on the way it is studied and followed-up. Never described clinical aspects such as toes abnormalities and hypospadias widen the range of dysmorphisms associated with this condition. Our data suggest that mutations may be implicated not only in impaired morphogenesis and hematopoiesis but also in progressive central nervous system damage, which remains to be further investigated and clarified.
我们报告了一名患有 -相关疾病的患者,首次全面展示了该疾病的临床和神经放射学进展过程,这可能对其研究和随访方式产生影响。从未描述过的临床特征,如脚趾异常和尿道下裂增宽了与此病症相关的畸形范围。我们的数据表明, 突变可能不仅与形态发生和造血功能受损有关,还与中枢神经系统的进行性损伤有关,这仍有待进一步研究和阐明。