Literature DB >> 23599883

Kocher debre semelaigne syndrome: a rare case report with orofacial manifestations.

Sunil R Panat1, Prakash Chandra Jha, Sangamesh N Chinnannavar, Ankkita Chakarvarty, Ashish Aggarwal.   

Abstract

Kocher Debre Semelaigne Syndrome is a rare syndrome with clinical manifestation of hypothyroidism associated with pseudomuscular hypertrophy. Very few cases have been reported on kocher-debre semelaigne syndrome in the literature with the incidence reported to be less than 10%. As per our knowledge; until now, only one case of oro-facial manifestations has been reported. Here we report one such case of Kocher debre semelaigne syndrome in an 11 year old boy, showing features of macroglossia, multiple impacted teeth, puffed lips and anterior open bite.

Entities:  

Keywords:  Hypothyroidism; Kocher Debre Semelaigne syndrome (KDSS); Myopathy; Orofacial aspects

Year:  2013        PMID: 23599883      PMCID: PMC3628204          DOI: 10.5001/omj.2013.33

Source DB:  PubMed          Journal:  Oman Med J        ISSN: 1999-768X


  13 in total

1.  Kocher-Debré-Sémélaigne syndrome.

Authors:  N Luiz
Journal:  Indian Pediatr       Date:  1998-11       Impact factor: 1.411

2.  Kocher Debre Semelaigne syndrome: regression of pesudohypertrophy of muscles on thyroxine.

Authors:  P Mehrotra; M Chandra; M K Mitra
Journal:  Arch Dis Child       Date:  2002-03       Impact factor: 3.791

3.  Kocher-Debre-Semelaigne syndrome.

Authors:  M P Bhide; M D Khare; A V Jaykar; A Y Ranade; P N Patnekar
Journal:  Indian Pediatr       Date:  1989-10       Impact factor: 1.411

4.  Kocher Debre Semelaigne syndrome mimicking primary muscle disease.

Authors:  A Virmani; A Gambhir; P U Iyer
Journal:  Indian Pediatr       Date:  1990-01       Impact factor: 1.411

5.  Kocher-Debre-Semelaigne syndrome.

Authors:  M Singh; G N Aram; S Azamy; L S Arya
Journal:  Indian Pediatr       Date:  1983-02       Impact factor: 1.411

6.  Kocher Debre Semelaigne syndrome.

Authors:  S P Khatua; A Gangwal; S Khatua
Journal:  Indian Pediatr       Date:  1984-04       Impact factor: 1.411

7.  Resolution of abnormal muscle enzyme studies in hypothyroidism.

Authors:  I Klein; P Mantell; M Parker; G S Levey
Journal:  Am J Med Sci       Date:  1980 May-Jun       Impact factor: 2.378

8.  Congenital anomalies in infant with congenital hypothyroidism.

Authors:  Zahra Razavi; Alireza Yavarikia; Saadat Torabian
Journal:  Oman Med J       Date:  2012-09

Review 9.  Unusual manifestations of hypothyroidism.

Authors:  I Klein; G S Levey
Journal:  Arch Intern Med       Date:  1984-01

10.  Kocher-debre-semelaigne syndrome: hypothyroid muscular pseudohypertrophy-a rare report of two cases.

Authors:  Chandan Shaw; Prachi Shaw
Journal:  Case Rep Endocrinol       Date:  2012-03-12
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  2 in total

1.  Case Report: The Specter of Untreated Congenital Hypothyroidism in Immigrant Families.

Authors:  Elwaseila Hamdoun; Peter Karachunski; Brandon Nathan; Melissa Fischer; Jane L Torkelson; Amy Drilling; Anna Petryk
Journal:  Pediatrics       Date:  2016-04-14       Impact factor: 7.124

Review 2.  Hypothyroid myopathy: A peculiar clinical presentation of thyroid failure. Review of the literature.

Authors:  Alessandro Sindoni; Carmelo Rodolico; Maria Angela Pappalardo; Simona Portaro; Salvatore Benvenga
Journal:  Rev Endocr Metab Disord       Date:  2016-12       Impact factor: 6.514

  2 in total

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