Marozio L
No ORCID on file
· 2 papers in corpus
· active 2022-2025
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Frequent coauthors
- Canosa S 2
- Maffei P 2
- Benedetto C 2
- Canuto EM 1
- Carosso M 1
- Dassie F 1
- Ditaranto S 1
- Gennarelli G 1
- Milan G 1
- Revelli A 1
2025
PurposeAlström syndrome (AS) is an extremely rare, autosomal recessive genetic disorder. Fertility implications are particularly relevant for women affected by AS, and no cases of patients achieving pregnancy and live birth with in vitro fe…
2022
Background: Alström syndrome (AS) is an ultrarare multisystemic progressive disease caused by autosomal recessive variations of the ALMS1 gene (2p13). AS is characterized by double sensory impairment, cardiomyopathy, childhood obesity, extr…