Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M. Sellouti"'
Publikováno v:
Asian Journal of Pediatric Research. :1-5
Triple X syndrome is a relatively common chromosomal abnormality affecting 0.1% of live-born girls. Most of these girls have a normal phenotype and only a few cases have birth defects. The diagnosis of triple X syndrome may never be made because the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fc1a19c99cc29a0a15940db2b9343b7
https://doi.org/10.9734/ajpr/2023/v11i2214
https://doi.org/10.9734/ajpr/2023/v11i2214
Publikováno v:
Scholars Journal of Medical Case Reports. 10:1118-1121
Pompe disease, is a rare severe, autosomal, recessive, and progressive genetic disorder caused by deficiency in alpha-glucosidase. The classic infantile-onset is the most broadly known form of Pompe disease, which presents with severe heart involveme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97602974c9eccd7f2273add0ffac4d16
https://doi.org/10.36347/sjmcr.2022.v10i11.013
https://doi.org/10.36347/sjmcr.2022.v10i11.013
Publikováno v:
Asian Journal of Pediatric Research. :32-36
Hydrops fetalis is defined by the accumulation of fluids in the serous membranes (pleurisy, ascites, pericarditis...), it is a rare condition; its etiologies are divided into immunological and non-immunological. Supraventricular tachycardia remains a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e3c8db2aa04fc7f2a8c03017809c887
https://doi.org/10.9734/ajpr/2022/v10i2194
https://doi.org/10.9734/ajpr/2022/v10i2194
Publikováno v:
Acta Scientific Paediatrics. 2:53-54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f534348efc816d462b58cb62d3d119b
https://doi.org/10.31080/aspe.2019.02.0170
https://doi.org/10.31080/aspe.2019.02.0170