Hypophosphatasia is an inherited genetic disease characterized by a deficit in alkaline phosphatase activity. Its clinical spectrum is extremely variable, and includes skeletal and dental malformations, depending on the severity of the disease. Oral repercussions are present at all stages of the disease, and affect all mineralized dental tissues. The early loss of teeth is linked to an aplasia of the acellular cementum, the area of insertion of the periodontal ligament. Other dental tissues are sometimes affected, and include hypomineralization of the alveolar bone, dentin and enamel. The pediatric dentist is in a privileged position in the early diagnosis of hypophosphatasia.L’hypophosphatasie est une maladie génétique héréditaire, caracté...
Hypophosphatasia is characterized by defective bone mineralization associated with impaired activity...
La hipofosfatasia es una enfermedad hereditaria autosómica recesiva o dominante que afecta a ambos s...
Hypophosphatasia (HPP) is caused by loss-of-function mutation(s) within the gene TNSALP that encodes...
Hypophosphatasia is an inherited genetic disease characterized by a deficit in alkaline phosphatase ...
L'hypophosphatasie est une maladie génétique, héréditaire, rare qui se manifeste principalement par ...
Dental anomalies exist in every subtype of hypophosphatasia (HPP), from the most severe to the most ...
Hypophosphatasia (HPP) is a rare genetic disease characterized by a decrease in the activity of tiss...
Hypophosphatasia (HPP) is a rare genetic disease characterized by a decrease in the activity of tiss...
Hypophosphatasia is a rare metabolic disorder which manifests characteristics such as abnormal miner...
L'hypophosphatasie est une maladie héréditaire rare (1/100 000), due au déficit ou à l'absence de l'...
International audienceBACKGROUND: Hypophosphatasia (HP) is a rare inherited disorder characterized b...
Hypophosphatasia (HPP) is a rare inherited metabolic disease in which mutations in the ALPL gene (en...
Hypophosphatasia is a hereditary disorder characterized by a deficiency of serum and bone alkaline p...
Hypophosphatasia (HPP) is a group of inherited disorders characterised by the impaired mineralisatio...
ALPL encodes tissue-nonspecific alkaline phosphatase (TNAP), an enzyme expressed in bone, teeth, liv...
Hypophosphatasia is characterized by defective bone mineralization associated with impaired activity...
La hipofosfatasia es una enfermedad hereditaria autosómica recesiva o dominante que afecta a ambos s...
Hypophosphatasia (HPP) is caused by loss-of-function mutation(s) within the gene TNSALP that encodes...
Hypophosphatasia is an inherited genetic disease characterized by a deficit in alkaline phosphatase ...
L'hypophosphatasie est une maladie génétique, héréditaire, rare qui se manifeste principalement par ...
Dental anomalies exist in every subtype of hypophosphatasia (HPP), from the most severe to the most ...
Hypophosphatasia (HPP) is a rare genetic disease characterized by a decrease in the activity of tiss...
Hypophosphatasia (HPP) is a rare genetic disease characterized by a decrease in the activity of tiss...
Hypophosphatasia is a rare metabolic disorder which manifests characteristics such as abnormal miner...
L'hypophosphatasie est une maladie héréditaire rare (1/100 000), due au déficit ou à l'absence de l'...
International audienceBACKGROUND: Hypophosphatasia (HP) is a rare inherited disorder characterized b...
Hypophosphatasia (HPP) is a rare inherited metabolic disease in which mutations in the ALPL gene (en...
Hypophosphatasia is a hereditary disorder characterized by a deficiency of serum and bone alkaline p...
Hypophosphatasia (HPP) is a group of inherited disorders characterised by the impaired mineralisatio...
ALPL encodes tissue-nonspecific alkaline phosphatase (TNAP), an enzyme expressed in bone, teeth, liv...
Hypophosphatasia is characterized by defective bone mineralization associated with impaired activity...
La hipofosfatasia es una enfermedad hereditaria autosómica recesiva o dominante que afecta a ambos s...
Hypophosphatasia (HPP) is caused by loss-of-function mutation(s) within the gene TNSALP that encodes...