Aim This study evaluated the oral health status of adult patients with hypophosphatasia (HPP). Materials and Methods Parameters of oral health assessment comprised decayed/missing/filled teeth (DMFT) index, probing pocket depth and clinical attachment level (CAL) as well as documentation of tooth loss and periodontal health status according to CCD/AAP criteria. Findings were compared with national reference data (DMS V survey) reporting oral health status in age‐related controls. Within‐group comparisons were made between the HPP patients harbouring one versus two alkaline phosphatase liver/bone/kidney type (ALPL) gene variants. Results Of 80 HPP patients (64 female) with a mean age of 46.4 years (range 24–78) and one (n = 55) or t...
Hypophosphatasia is a rare metabolic disorder which manifests characteristics such as abnormal miner...
Hypophosphatasia (HPP) is caused by loss-of-function mutation(s) within the gene TNSALP that encodes...
Introduction: Hypophosphatasia, a metabolic bone disease caused by a tissue-nonspecific alkaline pho...
Diese Studie evaluiert die Mundgesundheit von Hypophosphatasie (HPP)-Patienten und beinhaltet die Un...
International audienceBACKGROUND: Hypophosphatasia (HP) is a rare inherited disorder characterized b...
Hypophosphatasia (HPP) is a rare and intractable metabolic bone disease caused by mutations in the A...
Hypophosphatasia (HPP) is a rare inherited metabolic disease in which mutations in the ALPL gene (en...
Hypophosphatasia (HPP) is a rare, inherited, metabolic disease caused by deficient tissue non‐specif...
Hypophosphatasia (HPP) is a rare genetic disease characterized by a decrease in the activity of tiss...
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 genetic disease caused by one or several mutations in ALPL gene encodin...
AbstractIntroductionHypophosphatasia, a metabolic bone disease caused by a tissue-nonspecific alkali...
Background: Hypophosphatasia (HPP) is an inborn disease caused by pathogenic variants in ALPL. Low l...
Hypophosphatasia (HPP) is a group of inherited disorders characterised by the impaired mineralisatio...
Hypophosphatasia is a rare metabolic disorder which manifests characteristics such as abnormal miner...
Hypophosphatasia (HPP) is caused by loss-of-function mutation(s) within the gene TNSALP that encodes...
Introduction: Hypophosphatasia, a metabolic bone disease caused by a tissue-nonspecific alkaline pho...
Diese Studie evaluiert die Mundgesundheit von Hypophosphatasie (HPP)-Patienten und beinhaltet die Un...
International audienceBACKGROUND: Hypophosphatasia (HP) is a rare inherited disorder characterized b...
Hypophosphatasia (HPP) is a rare and intractable metabolic bone disease caused by mutations in the A...
Hypophosphatasia (HPP) is a rare inherited metabolic disease in which mutations in the ALPL gene (en...
Hypophosphatasia (HPP) is a rare, inherited, metabolic disease caused by deficient tissue non‐specif...
Hypophosphatasia (HPP) is a rare genetic disease characterized by a decrease in the activity of tiss...
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 genetic disease caused by one or several mutations in ALPL gene encodin...
AbstractIntroductionHypophosphatasia, a metabolic bone disease caused by a tissue-nonspecific alkali...
Background: Hypophosphatasia (HPP) is an inborn disease caused by pathogenic variants in ALPL. Low l...
Hypophosphatasia (HPP) is a group of inherited disorders characterised by the impaired mineralisatio...
Hypophosphatasia is a rare metabolic disorder which manifests characteristics such as abnormal miner...
Hypophosphatasia (HPP) is caused by loss-of-function mutation(s) within the gene TNSALP that encodes...
Introduction: Hypophosphatasia, a metabolic bone disease caused by a tissue-nonspecific alkaline pho...