Clinical and genetic analysis of a patient with Mowat-Wilson syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 465-468, 2021.
Artículo
en Chino
| WPRIM
| ID: wpr-879604
ABSTRACT
OBJECTIVE@#To summarize the clinical phenotype and genotype of a Chinese child affected with Mowat-Wilson syndrome (MWS).@*METHODS@#Clinical data of the patient were collected. The patient was analyzed by whole-exome sequencing (WES) as well as Sanger sequencing.@*RESULTS@#The patient was a male infant with recurrent fever and slow growth. He also had characteristic facies, recurrent spasm, and growth retardation. WES revealed that he has carried a heterozygous nonsense c.2609C>G (p.Ser870X) variant of the ZEB2 gene (30% mosaicism). Based on the American College of Medical Genetics and Genomics standards and guidelines, the variant was predicted to be pathogenic (PVS1+PS1+PS2+PM2).@*CONCLUSION@#The c.2609C>G variant of the ZEB2 gene probably underlay the MWS in this child. The mosaicism of the variant may explain his mild symptoms.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Facies
/
Enfermedad de Hirschsprung
/
Discapacidad Intelectual
/
Microcefalia
/
Mutación
Tipo de estudio:
Guía de Práctica Clínica
/
Estudio pronóstico
Límite:
Niño
/
Humanos
/
Lactante
/
Masculino
Idioma:
Chino
Revista:
Chinese Journal of Medical Genetics
Año:
2021
Tipo del documento:
Artículo
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