Results 131 to 140 of about 5,240 (183)
Cervical myelopathy in mucopolysaccharidosis type IV.
Clinical neuropathology, 1999 We describe our experience with 8 Italian patients having mucopolysaccharidosis type IV, diagnosed between 1 and 10 years of life, who presented odontoid hypoplasia causing cervical myelopathy. We discuss the possibility of cranio-cervical stabilization in order to reduce the neurological complications.
Rigante D. +3 more
openaire +4 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Hearing Patterns in Morquio's Syndrome (Mucopolysaccharidosis IV)
Archives of Otolaryngology, 1977The hearing status of 18 patients with Morquio's syndrome (mucopolysaccharidosis IV) was evaluated. All three patients under age 8 years had a conductive hearing loss. Fourteen of 15 patients 8 years of age and older had a mixed or sensorineural hearing loss; one had normal hearing. Six patients wore hearing aids. By the end of the first decade of life,
E D, Riedner, L S, Levin
openaire +2 more sources
Oral findings in the Morquio syndrome (mucopolysaccharidosis IV)
Oral Surgery, Oral Medicine, Oral Pathology, 1975The Morquio syndrome is characterized by a specific pattern of platyspondylia, corneal opacities, keratosulfate excretion in the urine, and dental abnormalities. Oral examinations were performed on twelve patients with the condition. The maxillary anterior teeth were widely spaced and flared.
L S, Levin, R J, Jorgenson, C F, Salinas
openaire +2 more sources
Ultrastructure of lymphocytes and skin in mucopolysaccharidosis IV A (Morquio Syndrome)
Brain and Development, 1981Contrary to the reported absence of lymphocytic vacuoles in Morquio syndrome, lysosomal vacuoles were demonstrated by electron microscopy in lymphocytes and dermal cells of a 2 1/2-year-old Turkish girl biochemically and clinically proven to have type A of MPS IV or Morquio syndrome.
K, Ikeda, U, Burck, H H, Goebel
openaire +2 more sources
Medizinische Genetik, 1994
Mucopolysaccharidosis (MPS) type IV (Morquio's disease) is clinically, genetically and biochemically very heterogeneous. The current classification on type A and B with established enzymatic deficiency and type C with unknown enzymatic defect only partially disclose heterogeneity of the Morquio disease.
Barišić, Ingeborg +2 more
openaire +2 more sources
Mucopolysaccharidosis (MPS) type IV (Morquio's disease) is clinically, genetically and biochemically very heterogeneous. The current classification on type A and B with established enzymatic deficiency and type C with unknown enzymatic defect only partially disclose heterogeneity of the Morquio disease.
Barišić, Ingeborg +2 more
openaire +2 more sources