Unusual facies with delayed development and multiple malformations in a 14-month-old boy.
- Author:
Tong LU
1
;
Yi WANG
Author Information
1. Department of Pediatric Neurology, Children's Hospital of Fudan University, Shanghai 201102, China. yiwang@shmu.edu.cn.
- Publication Type:Case Reports
- MeSH:
Abnormalities, Multiple;
diagnosis;
genetics;
Craniofacial Abnormalities;
diagnosis;
genetics;
Developmental Disabilities;
diagnosis;
Face;
abnormalities;
Hand Deformities, Congenital;
diagnosis;
genetics;
Humans;
Infant;
Intellectual Disability;
diagnosis;
genetics;
Male;
Nails, Malformed;
diagnosis;
genetics
- From:
Chinese Journal of Contemporary Pediatrics
2017;19(8):921-925
- CountryChina
- Language:Chinese
-
Abstract:
Schinzel-Giedion syndrome is a rare autosomal dominant genetic disease and has the clinical features of severe delayed development, unusual facies, and multiple congenital malformations. In this case report, a 14-month-old boy had the clinical manifestations of delayed development, unusual facies (prominent forehead, midface retraction, hypertelorism, low-set ears, upturned nose, and micrognathia), and multiple congenital malformations (including cerebral dysplasia, dislocation of the hip joint, and cryptorchidism). The karyotype analysis and copy number variations showed no abnormalities, and whole exon sequencing showed a de novo heterozygous missense mutation, c.2602G > A (p. D868N), in SETBP1 gene. Therefore, the boy was diagnosed with Schinzel-Giedion syndrome. Myoclonic seizures in this boy were well controlled by sodium valproate treatment, and his language development was also improved after rehabilitation treatment. Clinical physicians should improve their ability to recognize such rare diseases, and Schinzel-Giedion syndrome should be considered for children with unusual facies, delayed development, and multiple malformations. Gene detection may help with the diagnosis of this disease.
