2010 ICD-9-CM Diagnosis Code 728.3
Other specific muscle disorders
- Arthrogryposis marked by congenital contractures involving two or more different joints with ankylosis, hypoplasia of the attached musculature, and multiple pterygia. Several types are recognized: Myopathic type is relatively rare and is characterized by muscle changes with fixed flexion deformities of the limbs and gross deformities of the chest and spine. Nuropathic type presents fixed extension or flexion deformities of the limbs. Distal type affects the distal portions of the extremities. Distal arthrogryposis is further divided into two types: At least 3 varies of X-linked distal arthrogryposis are recognized: 1. Lethal form with severe contractures, scoliosis, chest deformities, micrognathia, and death by age of 3 months. Psychomotor retardation may occur. 2. A mild to moderate forms with blepharoptosis, microphallus, cryptorchidism, inguinal hernia, and normal intelligence. 3. A sporadic form with mild symptoms which gradually improve, which is manifested main by moderate contractures and normal intelligence. Type I involves primarily the distal parts of the hands and feet and is characterized by overlapping fingers, clenched fists, ulnar deviation of the fingers, camptodactyly, positional foot anomalies, and generally normal intelligence. Type II is divided into several subtypes and, in addition to arthrogryposis, has a variety of associated findings, including short stature, cleft lip and/or palate, scoliosis, trismus, and dull intellect.
- Short description: Muscle disorders NEC.
- ICD-9-CM 728.3 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
- You are viewing the 2010 version of ICD-9-CM 728.3.
- More recent version(s) of ICD-9-CM 728.3: 2011 2012 2013.
728.3 Alternative Terminology
728.3 Excludes 
)Applies To
Convert 728.3 to ICD-10-CM
ICD-9-CM Volume 2 Index entries containing back-references to 728.3:
multiplex, congenita 
psychogenic 
