Galactosialidosis (GS) is a rare form of lysosomal storage disease that involves a broad spectrum of skeletal and soft tissue abnormalities. We report here on a 4-year 7-month-old boy with mild mental retardation, exhibiting multiple caries cavities and associated infectious foci and macroglossia. A huge abdominal enlargement due to peritoneal ascites was evident. Behavioral management and patient positioning on the dental chair represented a true challenge. The patient was treated under general anesthesia. However, life-threatening postoperative complications occurred because of the impossibility of extubating the patient. A very careful preanesthetic assessment is crucial in children affected by general conditions associated with airway a...
This paper reports on previously undescribed dentofacial features a child suffering from Glycogen-St...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an uncommon inherited enzyme deficiency chara...
This paper presents a 12-year-old male patient with XXXXY syndrome, who was treated under general an...
Mucopolysaccharidosis (MPS) is a disorder of storage in which there is excessive accumulation of gly...
Glutaric aciduria type 1 (GA1) is a rare, inherited mitochondrial disorder that results from deficie...
AbstractGlutaric aciduria type 1 (GA1) is a rare, inherited mitochondrial disorder that results from...
Spinal muscular atrophies are inherited neurodegenerative disorders affecting anterior hem cells. Th...
Joubert syndrome is a rare type of autosomal recessive genetic disorder that the incidence of it has...
To pursue dental treatment in a child, needs an extra effort due to the need for behavior modificati...
Tooth inhalation remains a rare incident but it may occur during dental care, especially in children...
Although the majority of dental abscesses in children originate from dental caries or trauma, a few ...
Freeman-Sheldon syndrome (FSS) is a rare inherit-ed form of distal arthrogryposis characterized by c...
General anesthesia is often required for mentally retarded children undergoing extensive dental trea...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Gingival enlargement (GE) is a well-known clinical phenomena with the primary aetiology being plaque...
This paper reports on previously undescribed dentofacial features a child suffering from Glycogen-St...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an uncommon inherited enzyme deficiency chara...
This paper presents a 12-year-old male patient with XXXXY syndrome, who was treated under general an...
Mucopolysaccharidosis (MPS) is a disorder of storage in which there is excessive accumulation of gly...
Glutaric aciduria type 1 (GA1) is a rare, inherited mitochondrial disorder that results from deficie...
AbstractGlutaric aciduria type 1 (GA1) is a rare, inherited mitochondrial disorder that results from...
Spinal muscular atrophies are inherited neurodegenerative disorders affecting anterior hem cells. Th...
Joubert syndrome is a rare type of autosomal recessive genetic disorder that the incidence of it has...
To pursue dental treatment in a child, needs an extra effort due to the need for behavior modificati...
Tooth inhalation remains a rare incident but it may occur during dental care, especially in children...
Although the majority of dental abscesses in children originate from dental caries or trauma, a few ...
Freeman-Sheldon syndrome (FSS) is a rare inherit-ed form of distal arthrogryposis characterized by c...
General anesthesia is often required for mentally retarded children undergoing extensive dental trea...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Gingival enlargement (GE) is a well-known clinical phenomena with the primary aetiology being plaque...
This paper reports on previously undescribed dentofacial features a child suffering from Glycogen-St...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an uncommon inherited enzyme deficiency chara...
This paper presents a 12-year-old male patient with XXXXY syndrome, who was treated under general an...