Variability of expression of oral-facial-digital syndrome type I in 15 Saudi girls: Why is there a high rate of median cleft lip in the phenotype?

被引:0
作者
Al-Qattan, Mohammad M. [1 ,2 ]
机构
[1] King Saud Univ, Div Plast Surg, Riyadh, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Div Plast Surg, Riyadh 11211, Saudi Arabia
关键词
Arabs; Expression; Oral-facial-digital; Saudi; POLYCYSTIC KIDNEY-DISEASE; EPIDEMIOLOGY; ANOMALIES; PATIENT; PALATE; GENE; OFD1;
D O I
10.1177/229255031402200413
中图分类号
R61 [外科手术学];
学科分类号
摘要
BACKGROUND: It is well known that the incidence of nonsyndromal cleft lip and palate varies greatly according to ancestry: 0.3 to 0.4 per 1000 live births in blacks, one in 1000 in Caucasians, and two in 1000 in Asians and individuals from the central province of Saudi Arabia. Median cleft lip is a variable feature in oral-facial-digital syndrome type I (OFD-I). OBJECTIVE: To test the hypothesis that genetic factors may determine the lip phenotype in OFD-I patients. METHODS: A study involving 15 Saudi girls (from the central province of Saudi Arabia) with OFD-I showed a high rate (93.3%) of median cleft lip and palate. This rate in OFD-I patients is known to range from 33% to 56% in Caucasians and also known to be very low in blacks. The authors compared the rate of median cleft lip with or without cleft palate in the Arabian series (93.3%) with the rate in Caucasians and blacks. RESULTS: The difference in median cleft lip with or without cleft palate among the three groups was significant. CONCLUSION: This supports the hypothesis that ancestral genetic factors may determine the lip phenotype in OFD-I patients.
引用
收藏
页码:229 / 232
页数:4
相关论文
共 32 条
[1]   Cone-shaped epiphyses in the toes and trifurcation of the soft palate in oral-facial-digital syndrome type-I [J].
Al-Qattan, MM .
BRITISH JOURNAL OF PLASTIC SURGERY, 1998, 51 (06) :476-479
[2]   Classification of limb anomalies in oral-facial-digital syndromes [J].
AlQattan, MM ;
Hassanain, JMA .
JOURNAL OF HAND SURGERY-BRITISH AND EUROPEAN VOLUME, 1997, 22B (02) :250-252
[3]  
ANNEREN G, 1984, CLIN GENET, V26, P178
[4]   A case-control study of nonsyndromic oral clefts in Maryland [J].
Beaty, TH ;
Wang, H ;
Hetmanski, JB ;
Fan, YT ;
Zeiger, JS ;
Liang, KY ;
Chiu, YF ;
Vanderkolk, CA ;
Seifert, KC ;
Wulfsberg, EA ;
Raymond, G ;
Panny, SR ;
McIntosh, I .
ANNALS OF EPIDEMIOLOGY, 2001, 11 (06) :434-442
[5]   EPIDEMIOLOGY OF FACIAL CLEFTS IN THE CENTRAL PROVINCE OF SAUDI-ARABIA [J].
BORKAR, AS ;
MATHUR, AK ;
MAHALUXMIVALA, S .
BRITISH JOURNAL OF PLASTIC SURGERY, 1993, 46 (08) :673-675
[6]   Ciliary Biology: Understanding the Cellular and Genetic Basis of Human Cillopathies [J].
Cardenas-Rodriguez, Magdalena ;
Badano, Jose L. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2009, 151C (04) :263-280
[7]   FAMILIAL OROFACIODIGITAL SYNDROME TYPE-I PRESENTING AS ADULT POLYCYSTIC KIDNEY-DISEASE [J].
DONNAI, D ;
KERZINSTORRAR, L ;
HARRIS, R .
JOURNAL OF MEDICAL GENETICS, 1987, 24 (02) :84-87
[8]  
Driva T, 2004, Int J Paediatr Dent, V14, P61, DOI 10.1111/j.1365-263X.2004.00503.x
[9]   Characterization of the OFD1/Ofd1 genes on the human and mouse sex chromosomes and exclusion of Ofd1 for the Xpl mouse mutant [J].
Ferrante, MI ;
Barra, A ;
Truong, JP ;
Banfi, S ;
Disteche, CM ;
Franco, B .
GENOMICS, 2003, 81 (06) :560-569
[10]   Identification of the gene for oral-facial-digital type I syndrome [J].
Ferrante, MI ;
Giorgio, G ;
Feather, SA ;
Bulfone, A ;
Wright, V ;
Ghiani, M ;
Selicorni, A ;
Gammaro, L ;
Scolari, F ;
Woolf, AS ;
Sylvie, O ;
Bernard, LM ;
Malcolm, S ;
Winter, R ;
Ballabio, A ;
Franco, B .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) :569-576