Asphyxiating thoracic dysplasia (often called Jeune syndrome) is a rare genetic bone growth problem. It mainly affects the chest, ribs, spine, and the long ...

Benallegue-Lacete syndrome is an extremely rare birth condition that affects how the baby’s bones and skull grow before birth. It is also called a syndromic ...

Cloverleaf skull-asphyxiating thoracic dysplasia syndrome is an extremely rare genetic bone disorder that affects a baby before birth. In this syndrome, the ...

Kleeblattschadel deformity, also called cloverleaf skull, is a very rare birth problem where a baby’s skull looks like a three-lobed cloverleaf. This happens ...

Cloverleaf skull deformity is a very rare problem where a baby’s skull looks like a three-leaf clover when seen from the front. The head has three rounded ...

Cloverleaf skull syndrome is a rare problem where a baby’s skull grows in a three-lobed shape that looks like a cloverleaf. This happens because several soft ...

Clouston’s hidrotic ectodermal dysplasia is a rare inherited skin and hair condition. It mainly affects the hair, nails and the thick skin on the palms of the ...

Clouston syndrome is a rare condition that a person is born with. It mainly affects three things in the body: the hair, the nails, and the skin on the palms of ...

Omphalocele–cloacal exstrophy–imperforate anus–spinal defect syndrome is usually called OEIS complex. It is a very rare birth condition where a baby is born ...

Exstrophy of cloaca sequence is a very rare birth defect. It happens very early in pregnancy, when the baby is still an embryo. In this condition, the lower ...

Cloacal exstrophy is a very rare birth defect. It happens when a baby’s lower tummy (abdomen), bladder, intestines, bottom (anus), and sometimes the spine and ...

Wallis-Zieff-Goldblatt syndrome is an extremely rare genetic bone growth problem. It mainly affects the bones near the shoulders and the upper arms, and also ...

Rhizomelic shortness with clavicular defect is an extremely rare genetic bone condition. It mainly affects the upper parts of the arms and the collarbones ...

Cleidorhizomelic syndrome is an extremely rare genetic bone growth disorder (skeletal dysplasia). It mainly affects the upper parts of the arms and legs ...

Cleidocranial dysplasia, recessive form, is a very rare genetic bone disease. It mainly affects the skull, collarbones, teeth, spine, and growth of the body. ...

Marie-Sainton disease is another name for a rare bone and tooth disorder officially called cleidocranial dysplasia or cleidocranial dysostosis. In this ...

Craniocleidodysostosis (often called cleidocranial dysostosis or cleidocranial dysplasia) is a rare genetic condition that mainly affects how bones and teeth ...

Cleidocranial dysostosis (often called cleidocranial dysplasia) is a rare genetic condition that mainly affects how the bones and teeth grow and harden. In ...

Labium leporinum is a Latin medical name for “harelip,” which means a cleft lip. A cleft lip is a birth problem where there is a gap or split in the upper lip ...

“Harelip disease” is an old word for a birth difference where the upper lip does not join together in the middle before birth. Today doctors say cleft lip ...