عنوان المقالة: Pulmonary Alveolar microlithiasis.Report of two brothers with the same illness and review of literature
الاستاذ الدكتور حسين آل سردار | Hussain.Al Sardar | 4030
نوع النشر
مجلة علمية
المؤلفون بالعربي
المؤلفون بالإنجليزي
Hussain Al-Sardar 1, Dhaher J S Al-Habbo, Rami M A Al-Hayali
الملخص الانجليزي
Pulmonary alveolar microlithiasis (PAM) is a rare lung disease characterised by extensive deposition of calpospherites within the alveoli. The disease is caused by mutations in the gene SLC34A2 encoding sodium-dependent phosphate co-transporter. It is an autosomal recessive disease with sporadic cases worldwide. Most patients are asymptomatic at the time of diagnosis. It may progress slowly over years to respiratory failure and cor pulmonale.
تاريخ النشر
31/03/2014
الناشر
Hussain Al-Sardar 1, Dhaher J S Al-Habbo, Rami M A Al-Hayali
رقم المجلد
رقم العدد
رابط DOI
10.1136/bcr-2013-201300
الصفحات
2
الكلمات المفتاحية
Pulmonary,microlithiasis,alvolar
رجوع