Maroteaux-Lamy syndrome associated with growth hormone deficiency.

TitleMaroteaux-Lamy syndrome associated with growth hormone deficiency.
Publication TypeJournal Article
Year of Publication1995
AuthorsBüyükgebiz B, Eroğlu Y, Kovanlikaya I, Sen A, Büyükgebiz A
JournalJ Pediatr Endocrinol Metab
Volume8
Issue4
Pagination305-7
Date Published1995 Oct-Dec
ISSN0334-018X
KeywordsChild, Preschool, Consanguinity, Growth Hormone, Humans, Infant, Insulin, Levodopa, Magnetic Resonance Imaging, Male, Mucopolysaccharidosis VI
Abstract

Growth retardation is a common feature of mucopolysaccharide storage disorders, mostly considered to be a consequence of skeletal changes, Maroteaux-Lamy disease is a subtype of mucopolysaccharidosis, demonstrating somatic changes and skeletal deformities. We present a case with Maroteaux-Lamy disease associated with growth hormone deficiency. Magnetic resonance imaging study revealed marked signal changes in white matter due to the storage in brain and empty sella appearance in sellar region. In the presence of empty sella syndrome, hypothalamic-pituitary dysfunction due to the storage material may have led to growth hormone deficiency in this patient. Therefore, we recommend patients with mucopolysaccharidosis, especially those who have growth retardation, to be evaluated by hormonal and radiological studies.

DOI10.1515/jpem.1995.8.4.305
Alternate JournalJ Pediatr Endocrinol Metab
PubMed ID8821911
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065