Cleidorhizomelic Syndrome
Cleidorhizomelic syndrome is an extremely rare genetic bone growth disorder (skeletal dysplasia). It mainly affects the upper parts of the arms and legs (called “rhizomelic” limb segments) and the ...
Cleidorhizomelic syndrome is an extremely rare genetic bone growth disorder (skeletal dysplasia). It mainly affects the upper parts of the arms and legs (called “rhizomelic” limb segments) and the ...
Cleidocranial dysplasia, recessive form, is a very rare genetic bone disease. It mainly affects the skull, collarbones, teeth, spine, and growth of the body. In this form, a child usually gets one ...
Marie-Sainton disease is another name for a rare bone and tooth disorder officially called cleidocranial dysplasia or cleidocranial dysostosis. In this disease, some bones do not form properly, ...
Craniocleidodysostosis (often called cleidocranial dysostosis or cleidocranial dysplasia) is a rare genetic condition that mainly affects how bones and teeth grow. The collar bones (clavicles), skull ...
Cleidocranial dysostosis (often called cleidocranial dysplasia) is a rare genetic condition that mainly affects how the bones and teeth grow and harden. In this condition, some bones—especially the ...
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 because the lip did not join together ...
“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 instead, because “harelip” is now seen as ...
Congenital fissure of lip is another name for cleft lip. It means a baby is born with a split or gap in the upper lip. This gap happens very early in pregnancy when the parts of the baby’s upper lip ...
Cheiloschisis of the upper lip means a split or gap in the upper lip that is present from birth. It happens when the parts of the baby’s face that should join together in early pregnancy do not come ...
Cleft upper lip means there is a gap or split in the baby’s upper lip that did not join together properly before birth. The split can look like a small notch or a wide opening, and it may go up ...
Cleft palate–stapes fixation–oligodontia syndrome is a very rare birth (congenital) condition. In this syndrome, a baby is born with three main problems together: a cleft in the soft part of the roof ...
Mathieu-De Broca-Bony syndrome (also called cleft palate-short stature-vertebral anomalies syndrome) is a very rare genetic condition. It affects many parts of the body at the same time. The main ...
Cleft palate with short stature and vertebral anomaly syndrome is a very rare genetic disease. It affects many parts of the body at the same time, especially the mouth (palate), face, spine, height, ...
Cleft palate–short stature–vertebral anomalies syndrome is a very rare genetic condition. It affects many parts of the body at the same time. Children are born with a cleft palate (an opening in the ...
Cleft palate–lateral synechia syndrome (CPLS) is a very rare birth condition. In this syndrome, a baby is born with a cleft palate (a gap in the roof of the mouth) and one or more fibrous bands ...
Say-Barber-Hobbs syndrome is a very rare genetic condition that affects how a baby’s face, skull, growth, skeleton and some internal organs develop before birth. It is also called Say syndrome or ...
Cleft palate-large ears-small head syndrome is a very rare genetic condition that affects how a baby’s face, head, bones, kidneys, and brain develop before birth. It is mainly described by three key ...
Cleft Palate with or without Ankyloglossia is a birth difference where there is an opening (a “gap”) in the roof of the mouth because the tissues did not join together properly when the baby was ...
Cleft lip/palate–intestinal malrotation–cardiopathy syndrome is an extremely rare multiple congenital anomaly syndrome that affects the face, mouth, heart, intestines, limbs, and sometimes other ...
Syndactyly-ectodermal dysplasia-cleft lip/palate is a very rare genetic syndrome where three main problems occur together: parts of the fingers or toes are joined (syndactyly), the skin-hair-teeth ...