X-linked spinal muscular atrophy (SMAX2) caused by de novo c.1731C > T substitution in the UBA1 gene

作者：Jedrzejowska Maria^*; Jakubowska Pietkiewicz Elzbieta; Kostera Pruszczyk Anna

来源：Neuromuscular Disorders, 2015, 25(8): 661-666.

DOI：10.1016/j.nmd.2015.05.001

• SMAX2
• USA1 gene
• Arthrogryposis
• Hypotonia
• Arflexia
• Congenital fractures

Infantile X-linked spinal muscular atrophy (SMAX2) is a rare form of spinal muscular atrophy manifesting as severe hypotonia, areflexia, arthrogryposis, facial weakness and cryptorchidism, and frequently accompanied by bone fractures.
We present a male patient with SMAX2 who presented with typical symptoms at birth, preceded by reduced fetal movements in the second and third trimesters of pregnancy. Clinical examination revealed a myopathic face with a characteristic tent-shaped open mouth, tongue fibrillations, profound muscle weakness, areflexia, multiple contractures, mild skeletal abnormalities and cryptorchidism. In the first days of the patient's life, fractures of the right femur and right humerus were found; however, calcium phosphate metabolism and densitometric examination were normal. Molecular analysis revealed a de novo c.1731C>T substitution in the UBA1 gene, which was localized in exon 15, the specific hot spot for mutation.

• 出版日期2015-8