Literature DB >> 431989

Phalangeal cone shaped epiphysis of the hands (PhCSEH) and chronic renal disease--the conorenal syndromes.

A Giedion.   

Abstract

The phalangeal cone shaped epiphysis of the hands (PhCSEH) observed in the extended Saldino-Mainzer syndrome (SMS), including nephronophthisis, are typed in accordance with standard tables. Of the more than 40 known types, type 28 and/or 28A were found in all eight cases available for analysis, frequently also associated with types 38, 38A, 37 and others. Similar PhCSEH are also observed in asphyxiating thoracic dysplasia (ATD), as well as in some cases of peripheral dysostosis combined with dwarfism. The striking similarity of the PhCSEH formula in our eight cases and of some cases of ATD, all suffering from chronic renal disease, suggests a common pathogenetic pathway of these conditions. The collective name of "conorenal syndromes" is suggested.

Entities:  

Mesh:

Year:  1979        PMID: 431989     DOI: 10.1007/bf00973675

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


  13 in total

1.  Peripheral dysostosis associated with juvenile nephronophthisis.

Authors:  T M Chakera
Journal:  Br J Radiol       Date:  1975-09       Impact factor: 3.039

2.  Juvenile nephronophthisis associated with retinal pigmentary dystrophy, cerebellar ataxia, and skeletal abnormalities.

Authors:  M Popović-Rolović; N Calić-Perisíc; G Bunjevacki; D Negovanović
Journal:  Arch Dis Child       Date:  1976-10       Impact factor: 3.791

3.  Juvenile nephronophthisis associated with skeletal abnormalities and hepatic fibrosis.

Authors:  D G Robins; T A French; T M Chakera
Journal:  Arch Dis Child       Date:  1976-10       Impact factor: 3.791

4.  Asphyxiating thoracic dysplasia. Clinical, radiological, and pathological information on 10 patients.

Authors:  F Oberklaid; D M Danks; V Mayne; P Campbell
Journal:  Arch Dis Child       Date:  1977-10       Impact factor: 3.791

5.  Familial renal-retinal dystrophy.

Authors:  B Senior
Journal:  Am J Dis Child       Date:  1973-03

6.  Cone-shaped epiphyses (CSE) in siblings with hereditary renal disease and retinitis pigmentosa.

Authors:  R M Saldino; F Mainzer
Journal:  Radiology       Date:  1971-01       Impact factor: 11.105

7.  Familial nephropathy associatdd with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities.

Authors:  F Mainzer; R M Saldino; M B Ozonoff; H Minagi
Journal:  Am J Med       Date:  1970-10       Impact factor: 4.965

8.  The spherical index. A measure of the roundness of the femoral head.

Authors:  N Fredensborg
Journal:  Acta Radiol Diagn (Stockh)       Date:  1977-11

9.  Acrodysplasias peripheral dysostosis, acrodysostosis and Thiemann's disease.

Authors:  A Giedion
Journal:  Clin Orthop Relat Res       Date:  1976 Jan-Feb       Impact factor: 4.176

10.  The renal disease of thoracic asphyxiant dystrophy.

Authors:  A B Gruskin; H J Baluarte; M L Cote; I B Elfenbein
Journal:  Birth Defects Orig Artic Ser       Date:  1974
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  7 in total

1.  Can a hand radiograph indicate a special diagnosis in a child with chronic kidney disease? Answers.

Authors:  Eren Soyaltın; Belde Kasap-Demir; Caner Alparslan; Seçil Arslansoyu-Çamlar; Elif Perihan Öncel; Özgür Kırbıyık; Demet Alaygut; Önder Yavaşcan; Gamze Türe; Fatma Mutlubaş
Journal:  Pediatr Nephrol       Date:  2017-07-24       Impact factor: 3.714

2.  Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease.

Authors:  Miriam Schmidts; Valeska Frank; Tobias Eisenberger; Saeed Al Turki; Albane A Bizet; Dinu Antony; Suzanne Rix; Christian Decker; Nadine Bachmann; Martin Bald; Tobias Vinke; Burkhard Toenshoff; Natalia Di Donato; Theresa Neuhann; Jane L Hartley; Eamonn R Maher; Radovan Bogdanović; Amira Peco-Antić; Christoph Mache; Matthew E Hurles; Ivana Joksić; Marija Guć-Šćekić; Jelena Dobricic; Mirjana Brankovic-Magic; Hanno J Bolz; Gregory J Pazour; Philip L Beales; Peter J Scambler; Sophie Saunier; Hannah M Mitchison; Carsten Bergmann
Journal:  Hum Mutat       Date:  2013-05       Impact factor: 4.878

3.  The nephronophthisis complex. A clinicopathologic study in children.

Authors:  R Waldherr; T Lennert; H P Weber; H J Födisch; K Schärer
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1982

4.  Twins with senior-Loken syndrome.

Authors:  S Giridhar; R Padmaraj; Prabha Senguttuvan
Journal:  Indian J Pediatr       Date:  2006-11       Impact factor: 1.967

5.  Tricho-rhino-phalangeal syndrome type I in a Belgian family.

Authors:  L A Verbruggen; C Van Laere; J Lamoureux; R Van Tiggelen
Journal:  Clin Rheumatol       Date:  1987-06       Impact factor: 2.980

6.  Mutations in human IFT140 cause non-syndromic retinal degeneration.

Authors:  Mingchu Xu; Lizhu Yang; Feng Wang; Huajin Li; Xia Wang; Weichen Wang; Zhongqi Ge; Keqing Wang; Li Zhao; Hui Li; Yumei Li; Ruifang Sui; Rui Chen
Journal:  Hum Genet       Date:  2015-07-28       Impact factor: 4.132

Review 7.  Skeletal ciliopathies: a pattern recognition approach.

Authors:  Atsuhiko Handa; Ulrika Voss; Anna Hammarsjö; Giedre Grigelioniene; Gen Nishimura
Journal:  Jpn J Radiol       Date:  2020-01-21       Impact factor: 2.374

  7 in total

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