Urinary Mucopolysaccharides in a Case of Morquio Syndrome (Mucopolysaccharidosis Type IV)

1973 ◽  
Vol 1 (4) ◽  
pp. 847-848 ◽  
Author(s):  
D. A. APPLEGARTH ◽  
G. BOZOIAN ◽  
R. B. LOWRY
Keyword(s):  
Mucopolysaccharidosis Type ◽  
Type Iv ◽  
Morquio Syndrome

scholarly journals A 16-year-old Girl with Morquio Syndrome: A Case Report

2018 ◽  
Vol 8 (3) ◽  
pp. 266-269
Author(s):  
AKM Motiur Rahman Bhuiyan ◽  
Maftahul Jannat ◽  
Md Zilan Miah Sarker ◽  
Mohammad Tanvir Islam ◽  
Amit Roy Chowdhury
Keyword(s):  
Autosomal Recessive ◽  
Autosomal Recessive Disorder ◽  
Consanguineous Marriage ◽  
Mucopolysaccharidosis Type ◽  
Skeletal Deformity ◽  
Type Iv ◽  
Morquio Syndrome ◽  
Radiological Changes ◽  
Morquio Syndrome A ◽  
Medical University

Morquio syndrome is a rare autosomal recessive disorder of mucopolysaccharide metabolism, also called mucopolysaccharidosis type IV. We report a case of Morquio syndrome in a16-year- old girl of normal intelligence, who got herself admitted in Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh. The patient had short stature and skeletal deformity and she belonged to a non-consanguineous marriage of her parents. She was diagnosed on the basis of clinical features, typical radiological changes and positive urinary mucopolysaccharide screening test.Birdem Med J 2018; 8(3): 266-269

Therapies of mucopolysaccharidosis type IV A (Morquio syndrome type A)

2014 ◽  
Vol 111 (2) ◽  
pp. S105
Author(s):  
Shunji Tomatsu ◽  
Carlos J. Alméciga-Díaz ◽  
Hector Barbosa ◽  
Adriana M. Montaño ◽  
Tadao Orii
Keyword(s):  
Type A ◽  
Syndrome Type ◽  
Mucopolysaccharidosis Type ◽  
Type Iv ◽  
Morquio Syndrome

scholarly journals Child with mucopolysaccharidosis type IV: Morquio syndrome

2015 ◽  
Vol 6 (10) ◽  
pp. 658
Author(s):  
Ali Akhtar ◽  
Sabina Manandhar ◽  
Eswat Ahmad
Keyword(s):  
Mucopolysaccharidosis Type ◽  
Type Iv ◽  
Morquio Syndrome

scholarly journals Pediatric Dental Management of an Uncommon Case of Mucopolysaccharidosis Type IV A (Morquio A Syndrome): A Case Report of a Three-Year Follow-Up

2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Andrea Gómez-González ◽  
Miguel Ángel Rosales-Berber ◽  
Paola De Ávila-Rojas ◽  
Amaury Pozos-Guillén ◽  
Arturo Garrocho-Rangel
Keyword(s):  
Case Report ◽  
Mucopolysaccharidosis Type ◽  
Type Iv ◽  
Morquio A ◽  
Dental Management ◽  
Histochemical Tests ◽  
Morquio Syndrome ◽  
Uncommon Case ◽  
Morquio A Syndrome

Mucopolysaccharidosis type IV A or Morquio syndrome is an uncommon inherited metabolic condition caused by the deficient intralysosomal storage of glycosaminoglycans. Diagnosis is typically based on clinical examination, skeletal radiographs, and histochemical tests in blood cells or fibroblasts. It is characterized by evident skeletal deformities, poor joint mobility, severe growth deficit, occlusal anomalies, and enamel defects. The aim of the present clinical case report is to describe the general oral management provided to a 6-year-old female patient and its corresponding evolution for more than three years.

scholarly journals Mucopolysaccharidosis type IV: report of 5 cases of Morquio Syndrome

2022 ◽  
Vol 17 (2) ◽  
pp. 385-391
Author(s):  
Jorge Alejandro Cadena Arteaga ◽  
Fabricio Andres Lasso Andrade ◽  
Denny Marcela Achicanoy Puchana ◽  
Diana Fernanda Achicanoy Puchana ◽  
Gina Natalia Caicedo Morillo ◽  
...  
Keyword(s):  
Mucopolysaccharidosis Type ◽  
Type Iv ◽  
Morquio Syndrome
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