A patient with a PTPN11 gene variant complicated with Chiari I malformation and syringomyelia and a review of literatures.

Autor: Yi Z; Department of Pediatric Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China., Xue J; Department of Pediatric Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China., Song Z; Department of Pediatric Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China., Li F; Department of Pediatric Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China., Yang C; Department of Pediatric Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China., Zhang Y; Department of Pediatric Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Jazyk: angličtina
Zdroj: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience [Int J Dev Neurosci] 2025 Feb; Vol. 85 (1), pp. e10396. Date of Electronic Publication: 2024 Dec 09.
DOI: 10.1002/jdn.10396
Abstrakt: Background: According to previous literature reports, PTPN11 gene variants account for approximately 50% of Noonan syndrome (NS) cases and 85% of Leopard syndrome (LS) cases. Several patients who were diagnosed with NS or LS complicated with Chiari I malformation (CIM) and/or syringomyelia have been reported to have a PTPN11 variant. However, it is not always clear whether the association between CIM and/or syringomyelia and PTPN11 variants is real or random. We try to explain this phenomenon by reporting a clinical case and making a mini-review.
Methods: We retrospectively described a clinical case in detail and made a genetic test on the proband and her family members using whole-exome sequencing. And made a review of the related literatures.
Results: The patient was manifesting progressive abnormal gait and muscle weakness for more than 2 years before she was admitted to our hospital at the age of 5 years and 2 months. On examination, she looked frail and slender. She had short stature, mild intellectual disability, decreased muscle strength in the left limb, thinner left limb, left hollow foot and foot drop, weakened left knee and Achilles tendon reflexes and a positive left Babinski sign. She looked timid and had very little expressive language. MRI of the brain and spine revealed CIM and syringomyelia with hydrops. Cardiac ultrasonography revealed an ostium secundum defect. ECG examination showed no abnormalities. She received a spinal cavity subarachnoid shunt; the symptoms were relieved to some extent, and the cavity in the lumbar vertebrae was significantly reduced after the surgery. Genetic testing found a variant, c. 922A>G (p. Asn308Asp) in the PTPN11 gene. Both parents were wild-type at this locus. A literature review found that 31 patients with NS or LS were complicated with CIM, syringomyelia or both. Together with our patient, a total of six patients in this group had the PTPN11 gene variant. Among them, four were complicated with both CIM and syringomyelia, and two were complicated with CIM only.
Conclusions: We report another case with a PTPN11 variant that was complicated with both CIM and syringomyelia. It suggests that CIM and syringomyelia may be clinical manifestations of PTPN11 variation-related diseases. This phenomenon may be underrated due to limitations of genetic diagnostic methods in the past. We strongly suggest routine craniocerebral and spinal MRI scans and genetic testing for patients suspected of having NS or LS.
(© 2024 International Society for Developmental Neuroscience.)
Databáze: MEDLINE
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