1.
NASN Sch Nurse
; 29(2): 67-70, 2014 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24707654
2.
Eur J Pediatr
; 164(12): 772-4, 2005 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16041526
RESUMO
UNLABELLED: Mucolipidosis III is a genetically heterogeneous lysosomal disorder characterised by progressive symptoms and signs, the commonest being skeletal pain due to bony destruction. We describe a patient who developed severe destruction of the temporomandibular joints leading to difficulties with speech and feeding, necessitating gastrostomy insertion. CONCLUSION: Temporomandibular joint involvement has not been previously reported in mucolipidosis III.