icd-10 code for arthrogryposis

What is the ICD 10 code for arthrogryposis multiplex congenita?

Arthrogryposis multiplex congenita. Q74.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM Q74.3 became effective on October 1, 2018. This is the American ICD-10-CM version of Q74.3 - other international versions of ICD-10 Q74.3 may differ.

What are the characteristics of arthrogryposis?

Arthrogryposis marked by congenital contractures involving two or more different joints with ankylosis, hypoplasia of the attached musculature, and multiple pterygia.

What are the types of distal arthrogryposis?

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.

What does Q69 mean in arthrogryposis?

polydactyly ( Q69.-) syndactyly ( Q70.-) Arthrogryposis marked by congenital contractures involving two or more different joints with ankylosis, hypoplasia of the attached musculature, and multiple pterygia.

What is a arthrogryposis?

Arthrogryposis, also called arthrogryposis multiplex congenita (AMC), involves a variety of non-progressive conditions that are characterized by multiple joint contractures (stiffness) and involves muscle weakness found throughout the body at birth.

Is arthrogryposis a form of muscular dystrophy?

Arthrogryposis is characterized by multiple joint contractures caused by abnormalities of muscle (muscular dystrophy, congenital myopathies, congenital absence of muscle), abnormal nerve function or innervation (central nervous system malformations, congenital neuropathy, failure of nerves to form or myelinate, ...

What is the most common form of arthrogryposis?

Amyoplasia, characterized by a lack of or abnormal muscular growth, is the most common form of arthrogryposis. It is estimated that approximately 33% of people diagnosed with arthrogryposis have amyoplasia.

What type of disability is arthrogryposis multiplex congenital?

Arthrogryposis multiplex congenita refers to a variety of conditions that involve congenital limitation of joint movement. Intelligence is typically normal except when the arthrogryposis is caused by a disorder or syndrome that also affects intelligence.

What are the different types of arthrogryposis?

There are four types of arthrogryposis:Amyoplasia. Amyoplasia is the most common type of arthrogryposis. ... Distal Arthrogryposis. Distal arthrogryposis affects only a few joints, usually in the hands and feet. ... Classic Arthrogryposis. ... Syndromic Arthrogryposis. ... Open Reduction. ... Tenotomy. ... Osteotomy. ... Cast and braces.

What causes arthrogryposis?

The major cause of arthrogryposis is fetal akinesia (ie, decreased fetal movements) due to fetal abnormalities (eg, neurogenic, muscle, or connective tissue abnormalities; mechanical limitations to movement) or maternal disorders (eg, infection, drugs, trauma, other maternal illnesses).

What are common signs of arthrogryposis?

Symptoms of ArthrogryposisThin, weak (atrophied), stiff or missing muscles.Stiff joints due to extra tissue (fibrosis or fibrous ankylosis)Differences in the skin around their joints, such as webbing.

Is arthrogryposis a neuromuscular disorder?

Other Neuromuscular Disorders Arthrogryposis (OMIM #108120) is a descriptive term used to represent a broad group of diseases, which have contractures of the joints in more than one area of the body that are present at the time of birth [140].

Is arthrogryposis a neuromuscular disease?

How is Arthrogryposis Multiplex Congenita diagnosed? There are many neuromuscular causes of AMC. Abnormalities can be found in the nerve cells in the spinal cord, the nerves themselves, the junction between the nerve and muscle, and the muscles.

What is the prognosis for patients diagnosed with arthrogryposis?

The lifespan of an individual with arthrogryposis is usually normal but may be altered by heart defects or central nervous system problems. In general, the prognosis for children with amyoplasia is good, though most children require intensive therapy for years.

What causes distal arthrogryposis?

Distal arthrogryposis type 1 can be caused by mutations in at least two genes: TPM2 and MYBPC1. These genes are active (expressed) in muscle cells , where they interact with other muscle proteins to help regulate the tensing of muscle fibers (muscle contraction).

What condition does AMC Princess Ana have?

AMC Princess Ana is a happy, motivated, hilarious, and wicked smart AMCer (individual with a rare condition called Arthrogryposis Multiplex Congenita). Ana is thriving and showing the world she can do it all! Nana-Mommy is Ana's maternal grandmother but to Ana and the world, Nana is Ana's Mommy.

About the ICD-10 Code for Arthrogryposis

Q74.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

2012 ICD-9-CM Diagnosis Code 728.3

ICD-9-CM 728.3 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 728.3 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).

Definition of ICD-10 Q74.3 Arthrogryposis

Arthrogryposis multiplex congenital (AMC) is the congenital joint contracture in two or more areas of the body.

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