Fanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with congenital and hematological abnormalities. Literature regarding the anesthetic management in these patients is limited. A management of a developmental dislocation of the hip was described in a patient with fanconi anemia. Because of the heterogeneous nature, a patient with fanconi anemia should be established thorough preoperative evaluation in order to diagnose on clinical features. In conclusion, we preferred caudal anesthesia in this patient with fanconi anemia without thrombocytopenia, because of avoiding from N2O, reducing amount of anesthetic, existing microcephaly, hypothyroidism and elevated liver enzymes, providing postoperative analgesia, an...
BackgroundNeurodegeneration with brain iron accumulation (NBIA) forms agroup of rare hereditary dise...
Oral surgery in patients with bleeding disorders is associated with a high risk of bleeding during a...
Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short statur...
Fanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with congenital ...
AbstractFanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with con...
Fanconi anemia is the most common of the rare inherited bone marrow failure syndromes. It is caused ...
We had experienced a successful caudal anesthesia for the intramedullary nailing of fractured femur ...
Cystinosis is a lysosomal storage disorder which is characterized by abnormal accumulation of amino ...
SummaryBackground and objectivesHereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osl...
Introduction. Fanconi–Bickel syndrome (FBS) is a rare genetic condition characterized by extremely s...
Fanconi anemia (FA) is an autosomal recessive disease characterizedby the presence of bone marrow fa...
The authors present the case of a child with complex congenital heart defect, bilateral malformati...
Homocystinuria is a rare autosomal recessive genetic disease. It is caused by a deficiency in cystat...
Fanconi anemia is a genetically-transmitted disease caused by biallelic inactivating mutations in mo...
Friedreichs ataxia is a rare (1:50 000) autosomal recessively inherited neurodegenerative disorder. ...
BackgroundNeurodegeneration with brain iron accumulation (NBIA) forms agroup of rare hereditary dise...
Oral surgery in patients with bleeding disorders is associated with a high risk of bleeding during a...
Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short statur...
Fanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with congenital ...
AbstractFanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with con...
Fanconi anemia is the most common of the rare inherited bone marrow failure syndromes. It is caused ...
We had experienced a successful caudal anesthesia for the intramedullary nailing of fractured femur ...
Cystinosis is a lysosomal storage disorder which is characterized by abnormal accumulation of amino ...
SummaryBackground and objectivesHereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osl...
Introduction. Fanconi–Bickel syndrome (FBS) is a rare genetic condition characterized by extremely s...
Fanconi anemia (FA) is an autosomal recessive disease characterizedby the presence of bone marrow fa...
The authors present the case of a child with complex congenital heart defect, bilateral malformati...
Homocystinuria is a rare autosomal recessive genetic disease. It is caused by a deficiency in cystat...
Fanconi anemia is a genetically-transmitted disease caused by biallelic inactivating mutations in mo...
Friedreichs ataxia is a rare (1:50 000) autosomal recessively inherited neurodegenerative disorder. ...
BackgroundNeurodegeneration with brain iron accumulation (NBIA) forms agroup of rare hereditary dise...
Oral surgery in patients with bleeding disorders is associated with a high risk of bleeding during a...
Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short statur...