1.
Neuropediatrics
; 54(1): 31-36, 2023 02.
Artículo
en Inglés
| MEDLINE
| ID: mdl-36126956
RESUMEN
Alazami syndrome is a rare disorder with an autosomal recessive inheritance caused by pathogenic biallelic variants in the LARP7 gene. Clinically, it is mainly characterized by short stature, intellectual disability, and dysmorphic facial features. However, the phenotype is not yet well-defined because less than 50 cases have been described to date. Here, we report three new patients from two unrelated Spanish families who, in addition to the defined features of Alazami syndrome, also exhibit unique features that broaden the phenotypic spectrum of the syndrome. Moreover, we describe the novel frameshift variant c.690_699delins27 in the LARP7 gene, in which loss of function is a known mechanism of Alazami syndrome.
Asunto(s)
Discapacidad Intelectual , Microcefalia , Humanos , Discapacidad Intelectual/diagnóstico , Discapacidad Intelectual/genética , Discapacidad Intelectual/patología , Fenotipo , Microcefalia/genética , Mutación del Sistema de Lectura , Síndrome , Ribonucleoproteínas/genética
2.
Mov Disord Clin Pract
; 11(7): 894-896, 2024 Jul.
Artículo
en Inglés
| MEDLINE
| ID: mdl-38696267