Arthrogryposis-like syndrome means a baby or child has stiff, fixed joints in more than one body area at birth, and the overall picture resembles ...

Distal arthrogryposis type 6 (DA6) is a very rare genetic condition where babies are born with stiff joints in the hands and feet (contractures) and ...

Arthrogryposis–hyperkeratosis syndrome is an extremely rare genetic condition seen at birth. Babies are born with many stiff joints (called arthrogryposis) ...

Stoll–Alembik–Finck syndrome is a very rare genetic condition present from birth. Children have arthrogryposis (stiff joints and contractures in many body ...

Oculomelic amyoplasia is an ultra-rare, inherited condition where a baby is born with tight joints in the arms and legs (called arthrogryposis) plus ...

Illum syndrome is an extremely rare condition present at birth. Babies have many stiff joints (contractures), a very small, tight mouth that looks like a ...

Arthrogryposis Multiplex Congenita—Whistling Face Syndrome is a rare, present-from-birth condition that affects the way muscles, joints, head, and face ...

Arthrogryposis multiplex congenita (AMC) describes babies born with stiff joints (contractures) in at least two different body areas because the baby did not ...

Multiple congenital arthrogryposis is an umbrella term for conditions where a baby is born with stiff joints (contractures) in two or more body areas. The ...

“Congenital arthromyodysplasia” is an old medical label that appeared in mid-20th-century rheumatology papers. It described babies born with stiff, bent joints ...

Arthrogryposis Multiplex Congenita (AMC) is a group of rare conditions where a baby is born with stiff joints (contractures) in two or more body areas. ...

Arthrogryposis means a baby is born with joints that are stiff and cannot move well because they are stuck in a bent or straight position. Doctors call these ...

Johnson–Munson syndrome is an extremely rare birth condition first described in two siblings, and later recognized as a triad of problems: (1) missing or very ...

Antley-Bixler syndrome is a rare genetic condition that affects how the skull, face, arms, legs, and some internal organs form before birth. The skull bones ...

Iridogoniodysgenesis is a birth (congenital) condition where parts of the eye that control fluid drainage—the iris (the colored ring) and the trabecular ...

Anterior Segment Dysgenesis (ASD) is a group of birth-time eye conditions where the front parts of the eye (the clear window called the cornea, the colored ...

Familial ocular anterior segment mesenchymal dysgenesis means a baby is born with parts at the very front of the eye (the cornea, iris, drainage angle, and ...

Anterior segment ocular dysgenesis is a group of birth-time (congenital) eye conditions in which the front structures of the eye—cornea, iris, lens, the ...

Anterior segment mesenchymal dysgenesis (ASD) is a group of birth-present (congenital) conditions where the front part of the eye does not form normally in the ...

Anophthalmia/microphthalmia–esophageal atresia (AEG) syndrome is a rare genetic condition in which a baby is born with one or both eyes missing or very small ...