PT  - JOURNAL ARTICLE
AU  - Sebastian, Alphy A.
AU  - Ahsan, Auswaf K.
TI  - Progeria with post-streptococcal glomerulonephritis. A rare case report with differential diagnosis
DP  - 2013 Feb 01
TA  - Saudi Medical Journal
PG  - 190--194
VI  - 34
IP  - 2
4099  - http://smj.org.sa/content/34/2/190.short
4100  - http://smj.org.sa/content/34/2/190.full
SO  - Saudi Med J2013 Feb 01; 34
AB  - 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 this literature.