Literature DB >> 10771849

DeSanctis-Cacchione syndrome.

O P Mishra1, A M Tripathi, G P Katiyar.   

Abstract

We report a case of DeSanctis-Cacchione Syndrome presenting with unusual features like early onset of cutaneous lesions and optic atrophy.

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Mesh：

Year:  1997        PMID： 10771849     DOI： 10.1007/bf02752463

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


  4 in total

1.  EEG and CT abnormalities in xeroderma pigmentosum.

Authors:  T Mimaki; T Tagawa; J Tanaka; K Sato; H Yabuuchi
Journal:  Acta Neurol Scand       Date:  1989-08       Impact factor: 3.209

2.  Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair.

Authors:  J H Robbins; K H Kraemer; M A Lutzner; B W Festoff; H G Coon
Journal:  Ann Intern Med       Date:  1974-02       Impact factor: 25.391

3.  De-Sanctis cacchione syndrome.

Authors:  P C Mishra; R Singh
Journal:  Indian J Pediatr       Date:  1982 Nov-Dec       Impact factor: 1.967

4.  Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases.

Authors:  K H Kraemer; M M Lee; J Scotto
Journal:  Arch Dermatol       Date:  1987-02
  4 in total

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