183 top medical experts on Histiocytosis with joint contractures and sensorineural deafness across 14 countries and 5 U.S. states, including 15 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Histiocytosis with joint contractures and sensorineural deafness: Histiocytosis-lymphadenopathy plus syndrome is a group of conditions with overlapping signs and symptoms that affect many parts of the body.This group of disorders includes H syndrome , pigmented hypertrichosis with insulin-dependent diabetes mellitus (PHID) , Faisalabad histiocytosis , and familial Rosai-Dorfman disease (also known as familial sinus histiocytosis with massive lymphadenopathy or FSHML). These conditions were once thought to be distinct disorders; however, because of the overlapping features and shared genetic cause, they are now considered to be part of the same disease spectrum.While some affected individuals have signs and symptoms characteristic of one of these conditions, others have a range of features from two or more of the conditions. The pattern of signs and symptoms can vary, even within the same family.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Faisalabad histiocytosis,  and Hypogonadism With or Without Hearing Loss Heart Anomalies Hepatosplenomegaly with Hypertrichosis Cutaneous Hyperpigmentation,  Pigmented Hypertrichosis With Insulin-Dependent Diabetes Mellitus Syndrome


  

        

                    


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