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Quoted phrase not found in phrase index: "Highly arched eyebrow"
Page 1
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
Urquhart J, Roberts R, de Silva D, Shalev S, Chervinsky E, Nampoothiri S, Sznajer Y, Revencu N, Gunasekera R, Suri M, Ellingford J, Williams S, Bhaskar S, Clayton-Smith J. Urquhart J, et al. Am J Med Genet A. 2016 May;170A(5):1216-24. doi: 10.1002/ajmg.a.37564. Epub 2016 Jan 20. Am J Med Genet A. 2016. PMID: 26789649
The 3MC syndromes are a group of rare autosomal recessive disorders where the main clinical features are cleft lip and palate, hypertelorism, highly arched eyebrows, caudal appendage, postnatal growth deficiency, and genitourinary tract anomalies. ...
The 3MC syndromes are a group of rare autosomal recessive disorders where the main clinical features are cleft lip and palate, hypertelorism …
Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13.
Tharapel SA, Lewandowski RC, Tharapel AT, Wilroy RS Jr. Tharapel SA, et al. J Med Genet. 1986 Aug;23(4):310-5. doi: 10.1136/jmg.23.4.310. J Med Genet. 1986. PMID: 3746829 Free PMC article.
In the distal trisomy group, the common features included haemangioma, bushy eyebrows, long curled eyelashes, prominent nasal bridge, long philtrum, thin upper lip, highly arched palate, and hexadactyly. ...
In the distal trisomy group, the common features included haemangioma, bushy eyebrows, long curled eyelashes, prominent nasal bridge, …
Transcoronal eyebrow lift with concomitant upper blepharoplasty.
Ellenbogen R. Ellenbogen R. Plast Reconstr Surg. 1983 Apr;71(4):490-9. doi: 10.1097/00006534-198304000-00008. Plast Reconstr Surg. 1983. PMID: 6828583
A technique for eyebrow lift is presented which employs the eyebrow arch used by makeup artists to add subjectively to the operation and prevent the aesthetically displeasing result of a too highly arched brow. ...
A technique for eyebrow lift is presented which employs the eyebrow arch used by makeup artists to add subjectively to the ope …
A new syndrome with distinct facial and auricular malformations and dominant inheritance.
Simosa V, Penchaszadeh VB, Bustos T. Simosa V, et al. Am J Med Genet. 1989 Feb;32(2):184-6. doi: 10.1002/ajmg.1320320209. Am J Med Genet. 1989. PMID: 2929657
We report on a mother and son with high forehead; elongated and flattened face; arched, sparse eyebrows; short palpebral fissures; telecanthus; long nose and hypoplastic nostrils; long philtrum; microstomia; high, narrow palate; nasal speech; chin dimples; and a …
We report on a mother and son with high forehead; elongated and flattened face; arched, sparse eyebrows; short palpebral fissu …
Asymmetrical skull, ptosis, hypertelorism, high nasal bridge, clefting, umbilical anomalies, and skeletal anomalies in sibs: is Carnevale syndrome a separate entity?
Al Kaissi A, Klaushofer K, Safi H, Chehida FB, Ghachem MB, Chaabounni M, Hennekam RC. Al Kaissi A, et al. Am J Med Genet A. 2007 Feb 15;143(4):349-54. doi: 10.1002/ajmg.a.31610. Am J Med Genet A. 2007. PMID: 17236195
A group of syndromes, consisting of Malpuech syndrome, Michels syndrome, Carnevale syndrome, OSA syndrome, and Mingarelli syndrome share the combination of symptoms of highly arched eyebrows, ptosis, and hypertelorism, and vary in other symptoms such as asymm …
A group of syndromes, consisting of Malpuech syndrome, Michels syndrome, Carnevale syndrome, OSA syndrome, and Mingarelli syndrome share the …