|تاریخ چاپ: 1399/04/19|
|A Girl with Farber Disease Treated with BoneMarrow Transplantation|
|Author(s):||Naser Ali Mirhosseini*، Elham Farasat، Elnaz Sheikhpour|
Farber disease is a very rare autosomal recessive disease of lipid metabolism caused by deficient activity of lysosomal acid ceramidase. Symptoms can begin in the first year of life by a triad of painful and swollen joints and subcutaneous nodules, progressive hoarseness and variable central nervous system involvement.
A5 monthsold girl with subcutaneous nodules in limbs, pain and swelling in her fingers, Knees, elbow and hoarseness was referredto our clinic. She had neurodevelopment delay in walking and talking. Genetic analysiswas reported homozygosity for a c.830C>A mutation in exon 11 of N-Acylsphingosine Amidohydrolase 1 (ASAH1)gene. She diagnosed with Farber disease and treated with bone marrow transplantation. After that her signs and symptoms were improved and she could to walk.
Farber disease is associated with characteristics including swollen joints, subcutaneous nodules, progressive hoarseness and variable CNS involvement. Moreover, bone marrow transplantation improved these symptoms.
|Keywords:||Farber disease، Bone marrow transplantation، CNS involvement|
|Article Type:||Case Report|
|Published:||World Journal of Peri & Neonatology, Volume:1 Issue: 1, 2018|
|Full text:||PDF is available on the website.|