Literature DB >> 1749675

Perinatal lethal hypophosphatasia; clinical, radiologic and morphologic findings.

M Shohat1, D L Rimoin, H E Gruber, R S Lachman.   

Abstract

Clinical, radiographic and morphologic analysis of nineteen cases of perinatal (lethal) hypophosphatasia was performed. Three families each had two affected offspring. All of the patients had lethal short limb dwarfism with very soft calvaria. Other clinical findings included polyhydramnios, blue sclerae and spurs in the mid-portion of the forearms and lower legs. Considerable variability was found in the skeletal radiographs. In addition to the well known radiographic features such as generalized decrease in the size of ossified bones with some bones not ossified at all, other changes observed included: 1) marked variability in the amount of bone ossification; 2) variability between patients as to which bones were most severely affected; 3) unusually dense, round, flattened, butterfly shaped; and sagittally clefted vertebral bodies; 4) variability in femoral shape including "chromosome" like, "campomelic" like, and shortening with or without metaphyseal cupping or irregularities; 5) osteochondral projections (Bowdler spurs) of the midshaft of the fibula and ulna. Recognition of the marked clinical and radiographic variability in this autosomal recessive lethal skeletal dysplasia is important for accurate genetic counseling and prenatal diagnosis.

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Mesh:

Year:  1991        PMID: 1749675     DOI: 10.1007/bf02026677

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  18 in total

1.  Apparent dominant inheritance of hypophosphatasia.

Authors:  J L SILVERMAN
Journal:  Arch Intern Med       Date:  1962-08

2.  Adult hypophosphatasia dominant inheritance in a large kindred.

Authors:  M P Whyte; S L Teitelbaum; W A Murphy; L V Avioli
Journal:  Trans Assoc Am Physicians       Date:  1978

3.  The prominent falx cerebri: new ultrasonic observation in hypophosphatasia.

Authors:  C L Laughlin; T G Lee
Journal:  J Clin Ultrasound       Date:  1982-01       Impact factor: 0.910

4.  Isoenzymes of alkaline phosphatase in infantile hypophosphatasia.

Authors:  H D Mueller; R A Stinson; F Mohyuddin; J K Milne
Journal:  J Lab Clin Med       Date:  1983-07

5.  Histologic and ultrastructural studies on the mineralization process in hypophosphatasia.

Authors:  A Ornoy; G E Adomian; D L Rimoin
Journal:  Am J Med Genet       Date:  1985-12

6.  First trimester diagnosis of hypophosphatasia with a monoclonal antibody to the liver/bone/kidney isoenzyme of alkaline phosphatase.

Authors:  R C Warren; C F McKenzie; C H Rodeck; G Moscoso; D J Brock; L Barron
Journal:  Lancet       Date:  1985-10-19       Impact factor: 79.321

7.  Prenatal diagnosis of hypophosphatasia.

Authors:  B G Kousseff; R A Mulivor
Journal:  Obstet Gynecol       Date:  1981-06       Impact factor: 7.661

8.  Infantile hypophosphatasia: autosomal recessive transmission to two related sibships.

Authors:  C A Moore; J C Ward; M L Rivas; H L Magill; M P Whyte
Journal:  Am J Med Genet       Date:  1990-05

9.  Prenatal diagnosis of hypophosphatasia; genetic, biochemical, and clinical studies.

Authors:  R A Mulivor; M Mennuti; E H Zackai; H Harris
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025

10.  Prominent transverse (Bowdler) bone spurs as a diagnostic clue in a case of neonatal hypophosphatasia without metaphyseal irregularity.

Authors:  A E Oestreich; M K Bofinger
Journal:  Pediatr Radiol       Date:  1989
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  20 in total

1.  Hyperechoic metaphyses in hypophosphatasia: what does it mean?

Authors:  Marie Brasseur-Daudruy; Valentine Ickowicz; Sophie Degre; Eric Le Goupils; Danielle Eurin
Journal:  Pediatr Radiol       Date:  2007-12-15

2.  Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2.

Authors:  Areeg H El-Gharbawy; Joseph N Peeden; Ralph S Lachman; John M Graham; Stephen R Moore; David L Rimoin
Journal:  Am J Med Genet A       Date:  2010-01       Impact factor: 2.802

3.  The boneless neonate: a severe form of achondrogenesis type I.

Authors:  H J Jaeger; A Schmitz-Stolbrink; J Hulde; M Novak; K Roggenkamp; K Mathias
Journal:  Pediatr Radiol       Date:  1994

4.  Outcome of perinatal hypophosphatasia in manitoba mennonites: a retrospective cohort analysis.

Authors:  Edward C W Leung; Aizeddin A Mhanni; Martin Reed; Michael P Whyte; Hal Landy; Cheryl R Greenberg
Journal:  JIMD Rep       Date:  2013-04-12

Review 5.  Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment.

Authors:  Michael P Whyte
Journal:  Nat Rev Endocrinol       Date:  2016-02-19       Impact factor: 43.330

Review 6.  Disorders of phosphate homeostasis in children, part 1: primer on mineral ion homeostasis and the roles of phosphate in skeletal biology.

Authors:  Richard M Shore
Journal:  Pediatr Radiol       Date:  2022-05-10

Review 7.  How can calcium pyrophosphate crystals induce inflammation in hypophosphatasia or chronic inflammatory joint diseases?

Authors:  C Beck; H Morbach; P Richl; M Stenzel; H J Girschick
Journal:  Rheumatol Int       Date:  2008-09-28       Impact factor: 2.631

8.  Absence of recognition of low alkaline phosphatase level in a tertiary care hospital.

Authors:  E Maman; D Borderie; C Roux; K Briot
Journal:  Osteoporos Int       Date:  2015-10-07       Impact factor: 4.507

9.  Prevention of Lethal Murine Hypophosphatasia by Neonatal Ex Vivo Gene Therapy Using Lentivirally Transduced Bone Marrow Cells.

Authors:  Osamu Iijima; Koichi Miyake; Atsushi Watanabe; Noriko Miyake; Tsutomu Igarashi; Chizu Kanokoda; Aki Nakamura-Takahashi; Hideaki Kinoshita; Taku Noguchi; Shinichi Abe; Sonoko Narisawa; José Luis Millán; Takashi Okada; Takashi Shimada
Journal:  Hum Gene Ther       Date:  2015-11-19       Impact factor: 5.695

10.  Prosthetic rehabilitation of hypophosphatasia: a case report.

Authors:  Bora Bağiş; Esra Baltacioğlu; Elif Aydoğan; Evşen Tamam
Journal:  Cases J       Date:  2008-12-12
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