Literature DB >> 4780873

Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: a case report.

B Say, S Balci, T Pirnar, R Israel, M Atasu.   

Abstract

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Year:  1973        PMID: 4780873     DOI: 10.1007/bf00973228

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


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  9 in total

1.  FAMILIAL NEUROVISCERAL LIPIDOSIS. AN ANALYSIS OF EIGHT CASES OF A SYNDROME PREVIOUSLY REPORTED AS "HURLER-VARIANT," "PSEUDO-HURLER," AND "TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT".

Authors:  B H LANDING; F N SILVERMAN; J M CRAIG; M D JACOBY; M E LAHEY; D L CHADWICK
Journal:  Am J Dis Child       Date:  1964-11

2.  A CASE OF THE SMITH-LEMLI-OPITZ SYNDROME OF MULTIPLE CONGENITAL ANOMALIES IN ASSOCIATION WITH DYSPLASIA EPIPHYSIALIS PUNCTATA.

Authors:  R GIBSON
Journal:  Can Med Assoc J       Date:  1965-03-13       Impact factor: 8.262

3.  Trisomy of chromosomes 13-15 and 17-18: its association with infantile arteriosclerosis.

Authors:  R L ROSENFIELD; S BREIBART; H ISAACS; H D KLEVIT; W J MELLMAN
Journal:  Am J Med Sci       Date:  1962-12       Impact factor: 2.378

4.  Thirteen cases of alkaptonuria from one family tree with special reference to osteo-arthrosis alkaptonurica.

Authors:  Y ABE; N OSHIMA; R HATANAKA; T AMAKO; R HIROHATA
Journal:  J Bone Joint Surg Am       Date:  1960-07       Impact factor: 5.284

5.  Subglottic pseudotumor, laryngeal dysplasia, and chondrodysplasia calcificans congenita with a t(D;B) chromosomal translocation.

Authors:  A Valdmanis; J R Wilson; J D Mann; G Pearson; M W Shaw
Journal:  Ann Genet       Date:  1967-06

6.  Conradi's disease. Chondrodystrophia calcificans congenita, congenital stippled epiphyses.

Authors:  D E Comings; C Papazian; H R Schoene
Journal:  J Pediatr       Date:  1968-01       Impact factor: 4.406

7.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

8.  The roentgenographic features of the oto-palato-digital (OPD) syndrome.

Authors:  L O Langer
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1967-05

9.  The cerebro-hepato-renal syndrome (CHRS) (Zellweger's syndrome).

Authors:  A K Poznanski; J S Nosanchuk; J Baublis; J F Holt
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1970-06
  9 in total
  3 in total

1.  Keutel syndrome: a report of four cases.

Authors:  H E Khosroshahi; O Uluoğlu; R Olguntürk; C Başaklar
Journal:  Eur J Pediatr       Date:  1989-12       Impact factor: 3.183

Review 2.  Brachytelephalangy with sparing of the fifth distal phalanx: a feature highly suggestive of Keutel syndrome.

Authors:  Stephen F Miller
Journal:  Pediatr Radiol       Date:  2002-12-19

Review 3.  The Keutel syndrome. Report of a case and review of the literature.

Authors:  F Ziereisen; C De Munter; N Perlmutter
Journal:  Pediatr Radiol       Date:  1993
  3 in total

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