arthrogryposis multiplex congenita

Arthrogryposis multiplex congenita whistling face, also known as Illum syndrome.

Daw was originally diagnosed with a rare condition known as arthrogryposis multiplex congenita.

Arthrogryposis multiplex congenita pulmonary hypoplasia, also with a large number of synonyms.

At birth, multiple congenital contractures of large joints (arthrogryposis multiplex congenita) may be present.

Arthrogryposis and arthrogryposis multiplex congenita are sometimes used interchangeably.

Very rarely, an infant can be born with arthrogryposis multiplex congenita, secondary to profound intrauterine weakness.

She was born in Perth with arthrogryposis multiplex congenita, a condition that causes muscle weakness and joint stiffness.

Overton has arthrogryposis multiplex congenita, a medical condition which "causes muscle weakness and a tendency for bones to break easily."

Arthrogryposis multiplex congenita, distal type 2B, also known as Freeman-Sheldon syndrome variant.

Arthrogryposis multiplex congenita, distal type 1 (AMCD1).

Arthrogryposis multiplex congenita CNS calcification.

When arthrogryposis affects two or more different areas of the body, it is referred to as arthrogryposis multiplex congenita (AMC).

Arthrogryposis multiplex congenita neurogenic type (AMCN).

Arthrogryposis, also known as arthrogryposis multiplex congenita (AMC), is a rare congenital disorder that is characterized by multiple joint contractures and can include muscle weakness and fibrosis.

Pearson was born with arthrogryposis multiplex congenita and first came to public attention in 1980 when then-British Prime Minister Margaret Thatcher carried him up stairs in 10 Downing Street having awarded him a 'Children of Courage' medal.

Arthrogryposis Multiplex Congenita, Distal, Type IIA Camptodactyly-Cleft Palate-Clubfoot Distal Arthrogryposis, Type IIA None Gordon syndrome is an extremely rare disorder that belongs to a group of genetic disorders known as the distal arthrogryposes.