Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shaikhah AlDossary"'
Autor:
Khloud Mubark Alotaibi, Mohannad Alsuhaibani, Khalid S. Al-Essa, Ahmed Khamis Bamaga, Amnah S. Mukhtar, Ali Mohammed Alrumaih, Huda F. Al-Hasinah, Shaikhah Aldossary, Fouad Alghamdi, Mohamad-Hani Temsah, Norah Abanmy, Monira Alwhaibi, Yousif Asiri, Yazed AlRuthia
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundSpinal muscular atrophy (SMA) is a rare debilitating condition with a significant burden for patients and society. However, little is known about how it affects Saudi Arabia's population. The socioeconomic and medical characteristics of aff
Externí odkaz:
https://doaj.org/article/93269d5213e04f6f935a604668566766
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 429-433 (2021)
MEGDEL 3-methylglutaconic (MG) aciduria, deafness, encephalopathy, Leigh-like syndrome is an autosomal recessive disorder associated with infantile hypoglycemia, progressive psychomotor developmental delay, cerebellar atrophy with lesions in the basa
Externí odkaz:
https://doaj.org/article/92e140e7c71140a7992099dd9cdd64eb
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 429-433 (2021)
Case Reports in Neurology
Case Reports in Neurology
MEGDEL 3-methylglutaconic (MG) aciduria, deafness, encephalopathy, Leigh-like syndrome is an autosomal recessive disorder associated with infantile hypoglycemia, progressive psychomotor developmental delay, cerebellar atrophy with lesions in the basa
Autor:
Alaa Alghamdi, Shaikhah AlDossary, Ahmed N. Othman, Wala Alabdulqader, Fawzia Amer, Mona Ali, Momen Almomen, Fouad Alghamdi
IntroductionSpinal Muscular atrophy (SMA) is an inherited, neuromuscular disease which is characterized by the deterioration of spinal motor neurons, causing progressive muscular atrophy and weakening. It is an autosomal recessive disease with the ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f52829a87a5becd778afe44b0eb4ad9
https://doi.org/10.21203/rs.3.rs-1760703/v1
https://doi.org/10.21203/rs.3.rs-1760703/v1