Ultrastructure of lymphocytes and skin in mucopolysaccharidosis IV A (Morquio syndrome). 1981

K Ikeda, and U Burck, and H H Goebel

Contrary 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.

UI MeSH Term Description Entries
D008214 Lymphocytes White blood cells formed in the body's lymphoid tissue. The nucleus is round or ovoid with coarse, irregularly clumped chromatin while the cytoplasm is typically pale blue with azurophilic (if any) granules. Most lymphocytes can be classified as either T or B (with subpopulations of each), or NATURAL KILLER CELLS. Lymphoid Cells,Cell, Lymphoid,Cells, Lymphoid,Lymphocyte,Lymphoid Cell
D009085 Mucopolysaccharidosis IV Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme. Eccentro-Osteochondrodysplasia,Morquio's Disease,Eccentroosteochondrodysplasia,GALNS Deficiency,Galactosamine-6-Sulfatase Deficiency,MPS IV A,MPS IV B,MPS IVA,MPS IVB,Morquio A Disease,Morquio B Syndrome,Morquio Disease,Morquio Syndrome,Morquio Syndrome A,Morquio Syndrome B,Morquio Syndrome, Type B,Morquio's Disease Type B,Morquio's Syndrome,Morquio-B Disease,Mucopolysaccharidosis 4,Mucopolysaccharidosis 4B,Mucopolysaccharidosis Type IV,Mucopolysaccharidosis Type IV A,Mucopolysaccharidosis Type IV B,Mucopolysaccharidosis Type IVA,Mucopolysaccharidosis Type IVB,Deficiencies, GALNS,Deficiencies, Galactosamine-6-Sulfatase,Deficiency, GALNS,Deficiency, Galactosamine-6-Sulfatase,Disease, Morquio,Disease, Morquio A,Disease, Morquio's,Disease, Morquio-B,Eccentro Osteochondrodysplasia,Eccentro-Osteochondrodysplasias,Eccentroosteochondrodysplasias,GALNS Deficiencies,Galactosamine 6 Sulfatase Deficiency,Galactosamine-6-Sulfatase Deficiencies,IV, Mucopolysaccharidosis Type,IVs, Mucopolysaccharidosis Type,Morquio B Disease,Morquio Syndromes,Morquios Disease,Morquios Syndrome,Mucopolysaccharidosis 4Bs,Mucopolysaccharidosis Type IVBs,Mucopolysaccharidosis Type IVs,Syndrome A, Morquio,Syndrome, Morquio,Syndrome, Morquio B,Syndrome, Morquio's,Syndromes, Morquio,Type IV, Mucopolysaccharidosis,Type IVs, Mucopolysaccharidosis
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D001706 Biopsy Removal and pathologic examination of specimens from the living body. Biopsies
D012867 Skin The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS.

Related Publications

K Ikeda, and U Burck, and H H Goebel
January 1990, Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie,
K Ikeda, and U Burck, and H H Goebel
January 1979, Revista chilena de pediatria,
K Ikeda, and U Burck, and H H Goebel
June 2007, The Journal of the Association of Physicians of India,
K Ikeda, and U Burck, and H H Goebel
June 1993, Ophthalmic paediatrics and genetics,
K Ikeda, and U Burck, and H H Goebel
March 1992, Der Radiologe,
K Ikeda, and U Burck, and H H Goebel
March 1975, Oral surgery, oral medicine, and oral pathology,
K Ikeda, and U Burck, and H H Goebel
January 1998, Ryoikibetsu shokogun shirizu,
K Ikeda, and U Burck, and H H Goebel
October 1975, The Johns Hopkins medical journal,
K Ikeda, and U Burck, and H H Goebel
January 1981, La Pediatria medica e chirurgica : Medical and surgical pediatrics,
K Ikeda, and U Burck, and H H Goebel
February 2022, Radiology case reports,
Copied contents to your clipboard!