Cleft lip and palate with syndactyly and pili torti is a very rare genetic condition. Doctors group it inside the ectodermal dysplasia syndromes, which are disorders that affect tissues made from the ...
Cleft lip and cleft palate with ectodermal dysplasia syndrome is a rare condition where a baby is born with a split in the upper lip and/or roof of the mouth, together with problems of hair, teeth, ...
Cleft palate and cleft lip with deafness and sacral lipoma syndrome (also called Lowry–Yong syndrome) is a very rare genetic condition. It has been reported only in two brothers, so medical knowledge ...
Cleft lip/palate-hearing loss-sacral lipoma syndrome (also written as cleft lip/palate-deafness-sacral lipoma syndrome) is an extremely rare, inherited birth defect syndrome. It has three main ...
Cleft lip/palate–deafness–sacral lipoma syndrome is an extremely rare genetic condition. Children are born with a cleft lip and/or cleft palate, very severe (often profound) sensorineural deafness, ...
Cleft lip-alveolus-palate syndrome means that a baby is born with a continuous gap that starts in the upper lip, goes through the gum ridge where the teeth sit (the alveolus), and continues into the ...
Cleft lip–progressive retinopathy syndrome is a very rare birth condition. In this condition a baby is born with a cleft lip (a gap in the upper lip) and later develops a slowly worsening eye disease ...
Cleft lip–cone rod dystrophy syndrome is an extremely rare inherited condition in which a baby is born with a cleft lip, and later in life develops a progressive eye disease called cone-rod dystrophy ...
Cleft lip-retinopathy syndrome is an extremely rare congenital condition in which a baby is born with a cleft lip and later develops a slowly worsening disease of the retina (the light-sensing layer ...
Cleft lip and palate–craniofacial dysmorphism–congenital heart defect–deafness (hearing loss) syndrome is a very rare genetic condition. It affects how the face, heart, and ears form before birth. ...
Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome is a very rare genetic condition that changes how a baby’s face, mouth, heart, eyes, hands, feet, and ears ...
Disease of the cleft of the alveolar process of the maxilla usually means all the problems related to a bony gap in the tooth-bearing part of the upper jaw (the alveolar process) that happens as part ...
Cleft lip and alveolus means there is a gap (cleft) in the upper lip and in the gum ridge that holds the upper teeth (alveolar ridge). This gap can be small or very large. It may involve the base of ...
Asymmetry of the face and limbs with overgrowth means that one side of the body, or one part such as an arm, leg or part of the face, grows larger than the other side in a clear and abnormal way. ...
A lymphatic malformation of the face and neck is a soft, spongy swelling made from lymph vessels that grew in an abnormal way before birth. These vessels form small or large sacs filled with clear ...
Oculootofacial dysplasia is a very rare genetic condition that affects the eyes (“oculo”), ears (“oto”), and face (“facial”). Children are born with this condition. It causes special facial features ...
Burn-McKeown syndrome is a very rare genetic condition present from birth. Children with this syndrome usually have blocked or very narrow back parts of the nose (choanal atresia or stenosis). ...
Branchio-oculo-facial syndrome (often shortened to BOFS) is a rare genetic condition that affects how the face, neck, eyes, and sometimes ears and kidneys form before birth. In this condition, some ...
Cerebrooculonasal syndrome (also written cerebro-oculo-nasal syndrome, CONS) is a very rare birth condition where a baby is born with problems in three main areas: the brain (“cerebro”), the eyes ...
Cerebro-costo-mandibular syndrome (CCMS) is a very rare genetic condition that is present from birth. It mainly affects the jaw (mandible), the ribs, and the roof of the mouth (palate). Babies with ...
