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Arthrogryposis (Multiplex Congenita Distal Type-2)

Definition


Definition of Arthrogryposis (Multiplex Congenita Distal Type-2)
It is an extremely rare disorder that belongs to a group of genetic disorders known as the distal arthrogryposes. These disorders typically involve stiffness and impaired mobility of certain joints of the lower arms and legs (distal extremities) including the knees, elbows, wrists, and/or ankles. These joints tend to be permanently fixed in a bent or flexed position (contractures).

Symptoms


Symptoms of Arthrogryposis (Multiplex Congenita Distal Type-2)
It is characterized by the permanent fixation of several fingers in a flexed position (camptodactyly), abnormal bending inward of the foot (clubfoot or talipes), and, less frequently, incomplete closure of the roof of the mouth (cleft palate).

Causes


Causes of Arthrogryposis (Multiplex Congenita Distal Type-2)
Consult with your doctor.

Diagnosis


Diagnosis of Arthrogryposis (Multiplex Congenita Distal Type-2)
Consult with your doctor.

Treatment


Treatment of Arthrogryposis (Multiplex Congenita Distal Type-2)
Consult with your doctor.

Prognosis


Prognosis of Arthrogryposis (Multiplex Congenita Distal Type-2)
Consult with your doctor.

Prevention


Prevention of Arthrogryposis (Multiplex Congenita Distal Type-2)
Consult with your doctor.


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