low nasal bridge

См. также в других словарях:

• Achondroplasia — The most common form of short stature with disproportionately short limbs dwarfism with short arms and legs. Achondroplasia is caused by mutation in the fibroblast growth factor receptor 3 gene (FGFR3), which is located on chromosome 4 in… …   Medical dictionary

• Blepharophimosis — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 33297 ICD10 = ICD10|H|02|5|h|00, ICD10|Q|10|3|q|10 ICD9 = ICD9|374.46, ICD9|743.62 ICDO = OMIM = 110100 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D016569 Blepharophimosis is a… …   Wikipedia

• Dwarfism, achondroplastic — A genetic disorder of bone growth, achondroplasia is the most common cause of short stature with disproportionately short limbs dwarfism with short arms and legs. There is a typically large head with prominence of the forehead (frontal bossing),… …   Medical dictionary

• Williams syndrome — Infobox Disease Name = Williams syndrome Caption = DiseasesDB = ICD10 = ICD10|Q|93|8|q|90 ICD9 = ICD9|758.9 ICDO = OMIM = 194050 MedlinePlus = 001116 eMedicineSubj = ped eMedicineTopic = 2439 MeshID = D018980 Williams syndrome (WS; also Williams… …   Wikipedia

• Down syndrome — Pathol. a genetic disorder, associated with the presence of an extra chromosome 21, characterized by mild to severe mental retardation, weak muscle tone, a low nasal bridge, and epicanthic folds at the eyelids. Also, Down s syndrome. Formerly,… …   Universalium

• Cardiofaciocutaneous syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 30111 ICD10 = ICD9 = ICDO = OMIM = 115150 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Cardiofaciocutaneous Syndrome (CFC) is an extremely rare and serious genetic disorder.It is… …   Wikipedia

• Conradi-Hünermann syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 32527 ICD10 = ICD10|Q|77|3|q|65 ICD9 = ICD9|756.59 ICDO = OMIM = 302960 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Conradi Hünermann syndrome is a type of chondrodysplasia… …   Wikipedia

• CCD (cleidocranial dysostosis) — A genetic (inherited) disorder of bone development characterized by: {{}}Absent or incompletely formed collar bones (the “cleido “ part refers to the clavicles, the collar bones) The child with this disorder can bring its shoulders together or… …   Medical dictionary

• Cleidocranial dysostosis — A genetic (inherited) disorder of bone development characterized by: {{}}Absent or incompletely formed collar bones (the “cleido “ part refers to the clavicles, the collar bones) The child with this disorder can bring its shoulders together or… …   Medical dictionary

• Cleidocranial dysplasia — A genetic (inherited) disorder of bone development characterized by: {{}}Absent or incompletely formed collar bones (the “cleido “ part refers to the clavicles, the collar bones) The child with this disorder can bring its shoulders together or… …   Medical dictionary

• Craniocleidodysostosis — A genetic (inherited) disorder of bone development characterized by: {{}}Typical cranial and facial abnormalities with square skull, late closure of the sutures of the skull, late closure of the fontanels (the soft spots), low nasal bridge,… …   Medical dictionary