Encephalopathies with intracranial calcification in children: clinical and genetic characterization

Davide TondutiEmail author View ORCID ID profile,
Celeste Panteghini,
Anna Pichiecchio,
Alice Decio,
Miryam Carecchio,
Chiara Reale,
Isabella Moroni,
Nardo Nardocci,
Jaume Campistol,
Angela Garcia-Cazorla,
Belen Perez Duenas,
Cerebral Calcification International Study Group,
Luisa Chiapparini,
Barbara Garavaglia and
Simona Orcesi

Orphanet Journal of Rare Diseases201813:135

https://doi.org/10.1186/s13023-018-0854-y

Received: 26 February 2018
Accepted: 21 June 2018
Published: 16 August 2018

Abstract

Background

We present a group of patients affected by a paediatric onset genetic encephalopathy with cerebral calcification of unknown aetiology studied with Next Generation Sequencing (NGS) genetic analyses.

Methods

We collected all clinical and radiological data. DNA samples were tested by means of a customized gene panel including fifty-nine genes associated with known genetic diseases with cerebral calcification.

Results

We collected a series of fifty patients. All patients displayed complex and heterogeneous phenotypes mostly including developmental delay and pyramidal signs and less frequently movement disorder and epilepsy. Signs of cerebellar and peripheral nervous system involvement were occasionally present. The most frequent MRI abnormality, beside calcification, was the presence of white matter alterations; calcification was localized in basal ganglia and cerebral white matter in the majority of cases. Sixteen out of fifty patients tested positive for mutations in one of the fifty-nine genes analyzed. In fourteen cases the analyses led to a definite genetic diagnosis while results were controversial in the remaining two.

Conclusions

Genetic encephalopathies with cerebral calcification are usually associated to complex phenotypes. In our series, a molecular diagnosis was achieved in 32% of cases, suggesting that the molecular bases of a large number of disorders are still to be elucidated. Our results confirm that cerebral calcification is a good criterion to collect homogeneous groups of patients to be studied by exome or whole genome sequencing; only a very close collaboration between clinicians, neuroradiologists and geneticists can provide better results from these new generation molecular techniques.