| HSM Syndrome | juvenile-familial Endocrinopathy Hypoparathyroidism Addison's Disease Menillansis |
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| LCP Disease | Legg-Calve-Perthes Disease ? Stages of LCP Disease(= Juvenile Idiopathic AVN) &nb... |
| DJOA | dominant juvenile optic atrophy |
| FJN | familial juvenile nephrophthisis |
| JA | judgment analysis; juvenile atrophy; juxta-articular |
| juvenile xanthogranuloma | Single or multiple reddish to yellow papules or nodules, usually found in young children, consisting of dermal infiltration by histiocytes and Touton giant cells, with increasing fibrosis. Synonym: nevoxanthoendothelioma. (05 Mar 2000) |
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| familial juvenile nephrophthisis | <nephrology> A rare hereditary kidney disease characterised by the gradual loss of kidney function due to the presence of cysts in the renal medulla. Symptoms include high urine output (cannot concentrate the urine), weakness, weight loss, nocturia, fatigue and headache. There is no cure and usually progresses from chronic renal failure to end stage renal disease. (27 Sep 1997) |