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Results 1 - 10 of 12 for Congenital cleft nose
  1. FREM1 gene 
    ... been identified in people with a disorder called bifid nose, renal agenesis, and anorectal malformations syndrome, sometimes called ... particular tissues, resulting in the cleft nasal cartilage (bifid nose), missing kidneys (renal agenesis), narrowed or misplaced anal ...
    https://medlineplus.gov/genetics/gene/frem1 - Genetics
  2. Manitoba oculotrichoanal syndrome 
    ... nose appears to be divided into two halves (bifid nose).About 20 percent of people with Manitoba oculotrichoanal ...
    https://medlineplus.gov/.../manitoba-oculotrichoanal-syndrome - Genetics
  3. 3p deletion syndrome 
    ... jaw (micrognathia), droopy eyelids (ptosis), malformed ears or nose, and widely spaced ... 3p deletion syndrome is likely a ...
    https://medlineplus.gov/genetics/condition/3p-deletion-syndrome - Genetics
  4. Fryns syndrome 
    ... thick nasal tip, a long space between the nose and upper lip (a long philtrum), ... congenital diaphragmatic hernias, most children with Fryns syndrome do ...
    https://medlineplus.gov/genetics/condition/fryns-syndrome - Genetics
  5. Diamond-Blackfan anemia 
    ... eyelids (ptosis); a broad, flat bridge of the nose; small, low-set ears; and a small lower jaw ... agenerative anemia Congenital erythroid hypoplastic anemia Congenital hypoplastic ...
    https://medlineplus.gov/genetics/condition/diamond-blackfan-anemia - Genetics
  6. Spondylocarpotarsal synostosis syndrome 
    ... opening in the roof of the mouth (a cleft palate), hearing loss, thin tooth enamel, ... Congenital scoliosis with unilateral unsegmented bar Congenital synspondylism SCT ...
    https://medlineplus.gov/.../spondylocarpotarsal-synostosis-syndrome - Genetics
  7. Pallister-Killian mosaic syndrome 
    ... rounded forehead; a broad nasal bridge; a short nose; widely spaced eyes; ... are born with a congenital diaphragmatic hernia, which is a hole in the ...
    https://medlineplus.gov/.../pallister-killian-mosaic-syndrome - Genetics
  8. Myhre syndrome 
    ... deeply set eyes, a shortened distance between the nose and upper lip (a short ... at birth (congenital heart defects). Fibrosis in the heart and blood ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
  9. Peters plus syndrome 
    ... ears; narrow eyes; a long area between the nose and mouth (philtrum); and a pronounced double curve of ... syndrome is a new congenital disorder of glycosylation and involves defective Omicron-glycosylation ...
    https://medlineplus.gov/genetics/condition/peters-plus-syndrome - Genetics
  10. Spondyloepiphyseal dysplasia congenita 
    ... an opening in the roof of the mouth (cleft palate), a tongue that is placed further back than ... congenita associated with conductive hearing loss. Ear Nose Throat J. 2000 Mar;79(3):178-82. ...
    https://medlineplus.gov/.../spondyloepiphyseal-dysplasia-congenita - Genetics
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