delayed eruption
Look at other dictionaries:
delayed dentition — eruption of the first deciduous teeth after the end of the thirteenth month of life or eruption of the first permanent teeth after the seventh year of life. Called also retarded d., delayed eruption, and dentia tarda … Medical dictionary
eruption — 1. A breaking out, especially the appearance of lesions on the skin. 2. A rapidly developing dermatosis of the skin or mucous membranes, especially when appearing as a local manifestation of one of the exanthemata; an e. is characterized,… … Medical dictionary
Consequences of the April 2010 Eyjafjallajökull eruption — The eruption of Eyjafjallajökull … Wikipedia
2011 Puyehue-Cordón Caulle eruption — Coordinates: 40°35′25″S 72°07′02″W / 40.59028°S 72.11722°W / 40.59028; 72.11722 The 2011 Puyehu … Wikipedia
Polymorphous light eruption — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 10327 ICD10 = ICD10|L|56|4|l|55 ICD9 = ICD9|692.72 ICDO = OMIM = MedlinePlus = eMedicineSubj = derm eMedicineTopic = 342 MeshID = Polymorphous light eruption (PLE), or polymorphic light… … Wikipedia
dentition — The natural teeth, as considered collectively, in the dental arch; may be deciduous, permanent, or mixed. [L. dentitio, teething] artificial d. SYN: denture (1). deciduous d. SYN: deciduous tooth. delayed d. delayed eruption of the teeth … Medical dictionary
Aarskog-Scott syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29329 ICD10 = ICD10|Q|87|1|q|80 ICD9 = ICD9|759.89 ICDO = OMIM = 100050 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Aarskog Scott syndrome is an inherited disease characterized by … Wikipedia
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
Parry-Romberg syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 30151 ICD10 = ICD10|G|51|8|g|50 ICD9 = ICD9|349.89 ICDO = OMIM = 141300 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D005150 Parry Romberg syndrome (sometimes called just Romberg… … 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
