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Novel NR2F1 variants likely disrupt DNA binding: molecular modeling in two cases, review of published cases, genotype–phenotype correlation, and phenotypic expansion of the Bosch–Boonstra–Schaaf optic atrophy syndrome
- Source :
- Molecular Case Studies. 3:a002162
- Publication Year :
- 2017
- Publisher :
- Cold Spring Harbor Laboratory, 2017.
-
Abstract
- Bosch–Boonstra–Schaaf optic atrophy syndrome (BBSOAS) is a recently described autosomal dominant disorder caused by mutations in the NR2F1 gene. There are presently 28 cases of BBSOAS described in the literature. Its common features include developmental delay, intellectual disability, hypotonia, optic nerve atrophy, attention deficit disorder, autism spectrum disorder, seizures, hearing defects, spasticity, and thinning of the corpus callosum. Here we report two unrelated probands with novel, de novo, missense variants in NR2F1. The first is a 14-yr-old male patient with hypotonia, intellectual disability, optic nerve hypoplasia, delayed bone age, short stature, and altered neurotransmitter levels on cerebrospinal fluid testing. The second is a 5-yr-old female with severe developmental delay, motor and speech delay, and repetitive motion behavior. Whole-exome sequencing identified a novel missense NR2F1 variant in each case, Cys86Phe in the DNA-binding domain in Case 1, and a Leu372Pro in the ligand-binding domain in Case 2. The presence of clinical findings compatible with BBSOAS along with structural analysis at atomic resolution using homology-based molecular modeling and molecular dynamic simulations, support the pathogenicity of these variants for BBSOAS. Short stature, abnormal CNS neurotransmitters, and macrocephaly have not been previously reported for this syndrome and may represent a phenotypic expansion of BBSOAS. A review of published cases along with new evidence from this report support genotype–phenotype correlations for this disorder.
- Subjects :
- 0301 basic medicine
Genetics
Optic nerve hypoplasia
Macrocephaly
General Medicine
030105 genetics & heredity
Biology
medicine.disease
Bioinformatics
Short stature
Hypotonia
03 medical and health sciences
030104 developmental biology
Atrophy
Autism spectrum disorder
Speech delay
Intellectual disability
medicine
medicine.symptom
Subjects
Details
- ISSN :
- 23732873 and 23732865
- Volume :
- 3
- Database :
- OpenAIRE
- Journal :
- Molecular Case Studies
- Accession number :
- edsair.doi...........d7cbad35677f80bda32202eee833650a
- Full Text :
- https://doi.org/10.1101/mcs.a002162