Academic Journal
Aromatic L-Amino Acid Decarboxylase Deficiency: A Genetic Screening in Sicilian Patients with Neurological Disorders
| العنوان: | Aromatic L-Amino Acid Decarboxylase Deficiency: A Genetic Screening in Sicilian Patients with Neurological Disorders |
|---|---|
| المؤلفون: | Santa Paola, Sandro, Di Blasi, Francesco Domenico, Borgione, Eugenia, Lo Giudice, Mariangela, Giuliano, Marika, Pettinato, Rosa, Di Stefano, Vincenzo, Brighina, Filippo, Lupica, Antonino, Scuderi, Carmela |
| المساهمون: | Santa Paola, Sandro, Di Blasi, Francesco Domenico, Borgione, Eugenia, Lo Giudice, Mariangela, Giuliano, Marika, Pettinato, Rosa, Di Stefano, Vincenzo, Brighina, Filippo, Lupica, Antonino, Scuderi, Carmela |
| سنة النشر: | 2024 |
| المجموعة: | IRIS Università degli Studi di Palermo |
| مصطلحات موضوعية: | AADCD, neuromuscular defect, aromatic L-amino acid decarboxylase deficiency, cognitive deficit, Sicily |
| الوصف: | Aromatic L-amino acid decarboxylase deficiency (AADCd) is a rare autosomal recessive neurometabolic disorder caused by AADC deficiency, an enzyme encoded by the DDC gene. Since the enzyme is involved in the biosynthesis of serotonin and dopamine, its deficiency determines the lack of these neurotransmitters, but also of norepinephrine and epinephrine. Onset is early and the key signs are hypotonia, movement disorders (oculogyric crises, dystonia and hypokinesia), developmental delay and autonomic dysfunction. Taiwan is the site of a potential founder variant (IVS6+4A>T) with a predicted incidence of 1/32,000 births, while only 261 patients with this deficit have been described worldwide. Actually, the number of affected persons could be greater, given that the spectrum of clinical manifestations is broad and still little known. In our study we selected 350 unrelated patients presenting with different neurological disorders including heterogeneous neuromuscular disorders, cognitive deficit, behavioral disorders and autism spectrum disorder, for which the underlying etiology had not yet been identified. Molecular investigation of the DDC gene was carried out with the aim of identifying affected patients and/or carriers. Our study shows a high frequency of carriers (2.57%) in Sicilian subjects with neurological deficits, with a higher concentration in northern and eastern Sicily. Assuming these data as representative of the general Sicilian population, the risk may be comparable to some rare diseases included in the newborn screening programs such as spinal muscular atrophy, cystic fibrosis and phenylketonuria. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| Relation: | info:eu-repo/semantics/altIdentifier/pmid/38275615; info:eu-repo/semantics/altIdentifier/wos/WOS:001151923900001; volume:15; issue:1; firstpage:1; lastpage:10; numberofpages:10; journal:GENES; https://hdl.handle.net/10447/634935; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85183109456; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10815063/ |
| DOI: | 10.3390/genes15010134 |
| الاتاحة: | https://hdl.handle.net/10447/634935 https://doi.org/10.3390/genes15010134 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10815063/ |
| Rights: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.96555893 |
| قاعدة البيانات: | BASE |
| DOI: | 10.3390/genes15010134 |
|---|