Tricho-hepato-enteric syndrome: Difference between revisions

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{{CMG}}; {{AE}} {{ADI}}
{{CMG}}; {{AE}} {{ADI}}
==Overview==
==Overview==
It is a rare genetic disorder presenting in children less than 1 year of age.<ref>http://www.checkorphan.org/disease/tricho-hepato-enteric-syndrome</ref>
It is a rare [[genetic]] disorder presenting in children less than 1 year of age.<ref>http://www.checkorphan.org/disease/tricho-hepato-enteric-syndrome</ref>
==Pathophysiology==
==Pathophysiology==


* It is a genetic disorder with an autosomal recessive inheritance pattern.
* It is a genetic disorder with an [[autosomal recessive]] inheritance pattern.


*  Mutations in TTC37 which encodes the putative protein Thespin, have recently been associated with Tricho-Hepato-Enteric syndrome. <ref>http://www.ncbi.nlm.nih.gov/pubmed?term=21120949</ref>
[[Mutations]] in TTC37 which encodes the putative protein Thespin, have recently been associated with Tricho-Hepato-Enteric syndrome. <ref>http://www.ncbi.nlm.nih.gov/pubmed?term=21120949</ref>
==Natural History, Complications and Prognosis==
==Natural History, Complications and Prognosis==
* Prognosis is poor.   
* Prognosis is poor.   


*  Many patients die before the age of 5  due to infections or cirrhosis.  
*  Many patients die before the age of 5  due to [[infections]] or [[cirrhosis]].  


==Diagnosis==
==Diagnosis==
===Symptoms===
===Symptoms===


* Intractable diarrhea
* [[Failure to thrive]]


*  Intrauterine growth retardation
Intractable [[diarrhea]]
 
*  [[Intrauterine growth retardation]]


*  Hair  abnormalities - prominent forehead and cheeks, a broad nasal root and widely spaces eyes ([[hypertelorism]])
*  Hair  abnormalities - prominent forehead and cheeks, a broad nasal root and widely spaces eyes ([[hypertelorism]])


* Facial abnormalities - their hairs are woolly, easily removed and poorly pigmented
* Facial abnormalities - their hairs are woolly, easily removed and poorly pigmented
===Physical Examination===
* Signs of [[liver failure]]


===Laboratory Tests===
===Laboratory Tests===
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*  Biochemical analysis of hair reveal -  sulfur-deficient brittle hair
*  Biochemical analysis of hair reveal -  sulfur-deficient brittle hair


*  Abnormal antibody generation - T cell dysfuntion
*  Abnormal antibody generation - [[T cell]] dysfuntion


==Treatment==
==Treatment==
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* No specific treatment
* No specific treatment


*  Total parenteral nutrition may reduce symptoms of diarrhea
[[Total parenteral nutrition]] may reduce symptoms of diarrhea


*  Avoiding further damage to the liver  
*  Avoiding further damage to the [[liver]]


==References==
==References==

Revision as of 07:50, 29 July 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2]

Overview

It is a rare genetic disorder presenting in children less than 1 year of age.[1]

Pathophysiology

  • Mutations in TTC37 which encodes the putative protein Thespin, have recently been associated with Tricho-Hepato-Enteric syndrome. [2]

Natural History, Complications and Prognosis

  • Prognosis is poor.

Diagnosis

Symptoms

  • Hair abnormalities - prominent forehead and cheeks, a broad nasal root and widely spaces eyes (hypertelorism)
  • Facial abnormalities - their hairs are woolly, easily removed and poorly pigmented


Physical Examination

Laboratory Tests

Biopsy

  • Small bowel - villous atrophy with low or no mononuclear cell infiltration of the lamina propria
  • Microscopic analysis of the hair - twisted hairs of unequal size and different shapes

Other Diagnostic studies

  • Scanning electron microscopy of hair - hair budding
  • Biochemical analysis of hair reveal - sulfur-deficient brittle hair
  • Abnormal antibody generation - T cell dysfuntion

Treatment

  • No specific treatment
  • Avoiding further damage to the liver

References

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