faciodigitogenital dysplasia
1faciodigitogenital dysplasia — noun A rare genetic disorder causing defects in bones and cartilage, and characterised by abnormalities of the face, hands and genitals. Syn: Aarskog syndrome …
2Faciodigitogenital dysplasia — This disorder is characterized by multiple birth defects involving the face, fingers and genitalia. Features include wide spaced eyes (ocular hypertelorism), front facing (anteverted) nostrils, a broad upper lip, a malformed ( saddle bag )… …
3Dysplasia — Abnormal in form. From the Greek dys (bad, disordered, abnormal) and plassein (to form). For example, retinal dysplasia is abnormal formation of the retina during embryonic development. * * * Abnormal tissue development. SEE ALSO: heteroplasia.… …
4Dysplasia, faciodigitogenital — This disorder is characterized by multiple birth defects involving the face, fingers and genitalia. Features include wide spaced eyes (ocular hypertelorism), front facing (anteverted) nostrils, a broad upper lip, a malformed ( saddle bag )… …
5syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …
6Aarskog-Scott syndrome — This disorder is characterized by multiple birth defects including wide spaced eyes (ocular hypertelorism), front facing (anteverted) nostrils, a broad upper lip, a malformed ( saddle bag ) scrotum, and laxity of the ligaments resulting in… …
7Syndrome, Aarskog-Scott — This disorder is characterized by multiple birth defects including wide spaced eyes (ocular hypertelorism), front facing (anteverted) nostrils, a broad upper lip, a malformed ( saddle bag ) scrotum, and laxity of the ligaments resulting in… …
8hypertelorism — Abnormal distance between two paired organs. [hyper + G. tele, far off, + horizo, to separate, fr. horos, a boundary] Bixler type h. accompanying features are microtia and clefting of the lip, palate, and nose, mental deficiency, atresia of the …
9Aarskog-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 …
10Spitzer Haaransatz — bei einem 17jährigen Mädchen Spitzer Haaransatz beim Mann …
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