clinical and genetic aspects of hypophosphatasia - Orodental phenotype and genotype findings in all subtypes of hypophosphatasia
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Lieferung aus: Vereinigte Staaten von Amerika, Usually ships in 1-2 business days.
Von Händler/Antiquariat, super_star_seller.
Hypophosphatasia (HP)is a rare inherited disorder characterized by defective bone and teeth mineralization, deficiency of serum and bone alkaline phosphatase (AP)activity. The diagnosis is based on serum alkaline phosphatase essay and molecular analysis of the tissue non specific alkaline phosphatase (ALPL) gene. AP participates in tooth formation and is seen in dental and peridental cells. They are mainly seen in the following forms: infantile, childhood, adult and odontoHP. The dental clinical signs consist in mobility of teeth, premature and spontaneous loss of primary and/or permanent teeth without inflammation of the gums, and sometimes in localized enamel hypoplasia. In the milder forms, rarely diagnosed per se, premature exfoliation of teeth is a trigger sign which can leed to a possible diagnosis. In infantile and childhood hypophosphatasia, the anterior primary teeth are generally lost spontaneously before 3 years of age. In the adult forms, the medical history could elicit a memory of early loss of teeth in childhood. Dental management consists in early diagnosis, prevention and prosthodontics. Paperback, Label: VDM Verlag Dr. Müller, VDM Verlag Dr. Müller, Produktgruppe: Book, Publiziert: 2010-02-12, Studio: VDM Verlag Dr. Müller, Verkaufsrang: 14888888.

Lieferung aus: Niederlande, 5-10 werkdagen.
bol.com.
Hypophosphatasia (HP)is a rare inherited disorder characterized by defective bone and teeth mineralization, deficiency of serum and bone alkaline phosphatase (AP)activity. The diagnosis is based on serum alkaline phosphatase essay and molecular analysis of the tissue non specific alkaline phosphatase (ALPL) gene. AP participates in tooth formation and is seen in dental and peridental cells. They are mainly seen in the following forms: infantile, childhood, adult and odontoHP. The dental clinical... Hypophosphatasia (HP)is a rare inherited disorder characterized by defective bone and teeth mineralization, deficiency of serum and bone alkaline phosphatase (AP)activity. The diagnosis is based on serum alkaline phosphatase essay and molecular analysis of the tissue non specific alkaline phosphatase (ALPL) gene. AP participates in tooth formation and is seen in dental and peridental cells. They are mainly seen in the following forms: infantile, childhood, adult and odontoHP. The dental clinical signs consist in mobility of teeth, premature and spontaneous loss of primary and/or permanent teeth without inflammation of the gums, and sometimes in localized enamel hypoplasia. In the milder forms, rarely diagnosed per se, premature exfoliation of teeth is a trigger sign which can leed to a possible diagnosis. In infantile and childhood hypophosphatasia, the anterior primary teeth are generally lost spontaneously before 3 years of age. In the adult forms, the medical history could elicit a memory of early loss of teeth in childhood. Dental management consists in early diagnosis, prevention and prosthodontics.Taal: Engels;Afmetingen: 6x229x152 mm;Gewicht: 163,00 gram;Verschijningsdatum: februari 2010;ISBN10: 3639236734;ISBN13: 9783639236736; Engelstalig | Paperback | 2010.

Lieferung aus: Deutschland, zzgl. Versandkosten, sofort lieferbar.
Orodental phenotype and genotype findings in all subtypes of hypophosphatasia, Buch, Softcover.

Lieferung aus: Deutschland, Next Day, più spese di spedizione.
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Lieferung aus: Vereinigte Staaten von Amerika, 交貨類型: Free, 交付: 世界各地, 提供位置: 45014 Fairfield,OH,USA, 免費送貨.
Von Händler/Antiquariat, grandeagleretail.
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Lieferung aus: Vereinigtes Königreich Großbritannien und Nordirland, 10-15 business days.