Progeria with post-streptococcal glomerulonephritis
نویسندگان
چکیده
يمسج للاتعا نوسينشتاه ايريجورب دروفليج ةمزلاتم دعت يفحق بسانت مدعب فصتي .دللجا ةشاشهل مزلام رطيسم .رويطلا هطقتلا روهظو ،كفلا رغصو ،يننستلا رخأتو ،يهجو ينج يف افون يد ينج ةرفط وه يسيئرلا يثارولا بيعلا نأ امك 16 رمعلا نم غلبي ضيرم ةلاح ريرقتلا اذه فصي .LMNA يذلاو نوسينشتاه ايريجورب دروفليج ضارعأ روهظ عم ماع ضارعأ ترهظ امك .ريبك لكشب تايبدلأا يف ةلالحا فصو تم ةفلتخلما تاصيخشتلا ةشقانم تم امك .ضيرلما ىدل دبكلا مخضت .لاقلما اذه يف ليصفتلاب Hutchinson-Gilford progeria syndrome is a rare autosomal dominant disorder associated with skin fragility. It is characterized by craniofacial disproportion, delayed dentition, micrognathia, and plucked bird appearance. The genetic defect is mainly de nova mutation in the lamin A gene. This report describes a 16-year-old patient with classical features of progeria along with post-streptococcal glomerulonephritis. The symptoms of hepatomegaly were also present in the patient. The differential diagnoses of this lesion are also discussed in detail in
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Rare immune-mediated pneumonitis in association with post-streptococcal glomerulonephritis.
We describe the case of a 48-year-old man with an acute nephritis and respiratory failure. Clinical history, streptococcal antibody titres and renal biopsy led to a diagnosis of post-streptococcal glomerulonephritis. Respiratory investigations excluded pulmonary oedema and infection. We hypothesize that this man had a co-existing post-streptococcal glomerulonephritis and an immune-mediated pneu...
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