Acronyms

HPP

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HPPHigh Pressure Processing (cold pasteurization technique)
HPPHTTP (Hypertext Transfer Protocol) Parameter Pollution (cyber attacks)
HPPHigh Pressure Pasteurization
HPPHurricane Preparedness Plan (various organizations)
HPPHypophosphatasia (bone disease)
HPPHamiltonian Path Problem (graph theory)
HPPHazard Prevention Program (Canada)
HPPHypno-Peripheral Processing
HPPHeader C++
HPPHp Partner Portal
HPPHp Printer
HPPHigh Performance Package
HPPHead Phones President (band)
HPPHospital Preparedness Program
HPPHealth Promotion Practice (journal)
HPPHigh Performance Pharmacy (standards)
HPPHydro Power Plant
HPPHealth Privacy Project
HPPHome Purchase Plan (various locations)
HPPHealth Promotion Program
HPPHazardous Process Piping (Uniform Mechanical Code)
HPPHawaiian Paradise Park
HPPHuman Pancreatic Polypeptide
HPPHistoric Preservation Plan
HPPHandset Protection Plan
HPPHomogeneous Poisson Process
HPPHomebuyer Protection Plan
HPPHereditary Pyropoikilocytosis
HPPHeat Pump Programme (International Energy Agency)
HPPHigh Performance Polymer
HPPHousing Preservation Project
HPPHyperkalemic Periodic Paralysis
HPPHydro Production Partner (now Bilfinger Berger Industrial Services)
HPPHealth Professionals Program
HPPHewlett Packard Pavilion
HPPHIV Prevention Program
HPPHeat Pipe Performance
HPPHomeless Persons Program (Australia)
HPPHouseholds Passed (mass market broadband)
HPPHernieuwde Progressieve Partij (Renewed Progressive Party - Suriname)
HPPHigh Priority Program
HPPHonda Power Port
HPPHigh Price Point (sales; various companies)
HPPHub Protocol Processor
HPPHigh-Pulse Power
HPPC++ Header File Extension
HPPHydrology Pre- and Postprocessor
HPPHypercube Parallel Processing
HPPHigh Power Plant
HPPHigh Point of Pavement (plot plans-grade elevatio)
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References in periodicals archive
Alexion also has two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare metabolic disorders, hypophosphatasia (HPP) and lysosomal acid lipase deficiency (LAL-D).
Similarly, in October 2015, FDA had announced the approval of Strensiq, a drug that can be used for the treatment of perinatal, infantile and juvenile-onset hypophosphatasia, which is a metabolic disorder affecting multiple body systems.
SEDC needs to be differentiated from achondroplasia, hypothyroidism; and other dysplasias with universal platyspondyly in young children including metatropic dysplasia, thanatophoric dysplasia, achondrogenesis and hypophosphatasia. Typical findings of achondroplasia are short rectangular vertebral bodies with relatively wide disk spaces and narrowing of the distal lumbar spinal canal.
Alexion also has two innovative enzyme replacement therapies for patients with life-threatening and ultra-rare metabolic disorders, hypophosphatasia and lysosomal acid lipase deficiency (LAL-D).
The company also has two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare metabolic disorders, hypophosphatasia and lysosomal acid lipase deficiency (LAL-D).
Hypophosphatasia It shows palmoplantar keratoderma along with progressive periodontitis.
In this case, the raised PLP, together with hypophosphatasemia and a history of recurrent fractures, was consistent with a diagnosis of hypophosphatasia (HPP).
None of the three cases history of corticosteroid use, and there were no findings about hypophosphatasia or osteogenesis imperfecta.
In hypophosphatasia, a congenital condition due to a mutation in ALPL, decreased ALP levels lead to excess accumulation of inorganic pyrophosphatases (12).
Hypophosphatasia (HPP) is a rare, inherited metabolic bone disorder characterized by low serum alkaline phosphatase (ALP) activity and impaired bone mineralization [1].
Hypophosphatasia (HPP) (OMIM# 241500, 241510, 146300) is a rare hereditary metabolic disease characterized by deficiency of alkaline phosphatase (ALP) due to mutations in the gene coding tissue non-specific ALP (TNSALP) enzyme (1p36.1-34) (1).
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