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A Case Report on Holt Oram Syndrome

Holt Oram Syndrome (HOS) falls in rare prevalence category with probability of 0.7 in 100,000 live births. It is a rare autosomal dominant multiple malformation syndrome characterized by abnormalities affecting hands, wrists, arms,congenital heart defects and/or conduction problems. Genetic mutatio...

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Detalles Bibliográficos
Principais autores: Ali Nawaz Khan, Erum Shahzadi Malik, Syed Onaiz Anwar, Amjad Mahmood, Jamal Azfar Khan
Formato: Artigo
Idioma:Inglês
Publicado: Army Medical College Rawalpindi 2022-11-01
Series:Pakistan Armed Forces Medical Journal
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Acceso en liña:https://pafmj.org/index.php/PAFMJ/article/view/9573
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