Congenital generalized lipodystrophy: identification of novel variants and expansion of clinical spectrum

被引:21
作者
Haghighi, A. [1 ,2 ,3 ,4 ,6 ]
Kavehmanesh, Z. [5 ]
Haghighi, A. [1 ,2 ,3 ,4 ,6 ]
Salehzadeh, F. [7 ]
Santos-Simarro, F. [8 ,9 ]
Van Maldergem, L. [10 ]
Cimbalistiene, L. [11 ]
Collins, F. [12 ]
Chopra, M. [13 ]
Al-Sinani, S. [14 ]
Dastmalchian, S. [15 ]
de Silva, D. C. [16 ]
Bakhti, H. [17 ]
Garg, A. [18 ,19 ]
Hilbert, P. [20 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, 77 Ave Louis Pasteur, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Howard Hughes Med Inst, 75 Francis St, Boston, MA 02115 USA
[4] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
[5] Baqiyatallah Univ Med Sci, Res Ctr Gastroenterol & Liver Dis, Tehran, Iran
[6] Univ Toronto, Toronto Gen Hosp, Toronto, ON M5G 1L7, Canada
[7] Ardabil Univ Med Sci, Bouali Hosp, Dept Pediat, Ardebil, Iran
[8] ISCIII, CIBERER, Ctr Invest Biomed Red Enfermedades Raras, Madrid, Spain
[9] UAM, Clin Genet Unit, INGEMM, IdiPAZ,Hosp Univ La Paz, Madrid, Spain
[10] Univ Franche Comte, Ctr Genet Humaine, F-25030 Besancon, France
[11] Vilnius Univ, Dept Human & Med Genet, Vilnius, Lithuania
[12] Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW, Australia
[13] Royal Prince Alfred Hosp, Dept Med Genom, Camperdown, NSW 2050, Australia
[14] Sultan Qaboos Univ Hosp, Dept Child Hlth, Gastroenterol Unit, Muscat, Oman
[15] Case Western Reserve Univ, Case Med Ctr, Cleveland, OH 44106 USA
[16] Univ Kelaniya, Dept Physiol, Fac Med, Ragama, Sri Lanka
[17] Takht E Jamshid Hosp, Dept Pathol, Karaj, Iran
[18] Univ Texas SW Med Ctr Dallas, Div Nutr & Metab Dis, Dept Internal Med, Dallas, TX 75390 USA
[19] Univ Texas SW Med Ctr Dallas, Ctr Human Nutr, Dallas, TX 75390 USA
[20] Inst Pathol & Genet, Gosselies, Belgium
关键词
AGPAT2; BSCL2; CGL1; CGL2; congenital generalized lipodystrophy; genotype-phenotype correlations; novel variants; BERARDINELLI-SEIP SYNDROME; PROTEIN SEIPIN; PTRF MUTATIONS; AGPAT2; CARDIOMYOPATHY; HETEROGENEITY; GENES; DIFFERENTIATION; DEFICIENCY; BSCL2;
D O I
10.1111/cge.12623
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Congenital generalized lipodystrophy (CGL) is an autosomal recessive disorder with two major subtypes. Variants in AGPAT2 result in CGL type 1 with milder manifestations, whereas BSCL2 variants cause CGL type 2 with more severe features. Muscle hypertrophy caused by lack of adipose tissue is present early in life in CGL patients. Our aim was to investigate 10 CGL patients from 7 different countries and report genotype-phenotype relationships. Genetic analysis identified disease-causing variants in AGPAT2 (five patients) and in BSCL2 (five patients), including three novel variants; c.134C>A (p.Ser45*), c.216C>G (p.Tyr72*) in AGPAT2 and c.458C>A (p.Ser153*) in BSCL2. We also report possible novel clinical features such as anemia, breast enlargement, steatorrhea, intraventricular hemorrhage and nephrolithiasis in CGL patients. Generalized lipodystrophy and muscular hypertrophy were the only features in all of our patients. Hepatomegaly was the second common feature. Some manifestations were exclusively noticed in our CGL2 patients; hypertrichosis, high-pitched voice and umbilical hernia. Bone cysts and history of seizures were noticed only in CGL1 patients. The findings of this study expand our knowledge of genotype-phenotype correlations in CGL patients. These results have important clinical applications in diagnosis and management of the CGL patients as well as in genetic counseling in families at-risk.
引用
收藏
页码:434 / 441
页数:8
相关论文
共 43 条
[1]   The metabolic syndrome and uric acid nephrolithiasis: Novel features of renal manifestation of insulin resistance [J].
Abate, N ;
Chandalia, M ;
Cabo-Chan, AV ;
Moe, OW ;
Sakhaee, K .
KIDNEY INTERNATIONAL, 2004, 65 (02) :386-392
[2]   Congenital generalized lipodystrophy: significance of triglyceride biosynthetic pathways [J].
Agarwal, AK ;
Garg, A .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2003, 14 (05) :214-221
[3]   Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy [J].
Agarwal, AK ;
Simha, V ;
Oral, EA ;
Moran, SA ;
Gorden, P ;
O'Rahilly, S ;
Zaidi, Z ;
Gurakan, F ;
Arslanian, SA ;
Klar, A ;
Ricker, A ;
White, NH ;
Bindl, L ;
Herbst, K ;
Kennel, K ;
Patel, SB ;
Al-Gazali, L ;
Garg, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (10) :4840-4847
[4]   AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34 [J].
Agarwal, AK ;
Arioglu, E ;
de Almeida, S ;
Akkoc, N ;
Taylor, SI ;
Bowcock, AM ;
Barnes, RI ;
Garg, A .
NATURE GENETICS, 2002, 31 (01) :21-23
[5]   Genetic disorders of adipose tissue development, differentiation, and death [J].
Agarwal, Anil K. ;
Garg, Abhimanyu .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2006, 7 :175-199
[6]   Berardinelli-Seip syndrome in a 6-year-old boy [J].
Babu, Priya ;
Sharma, Rakesh ;
Jayaseelan, Elizabeth ;
Appachu, Divya .
INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, 2008, 74 (06) :644-646
[7]   Congenital generalized lipodystrophy: A case report with neurological involvement [J].
Ben Turkia, H. ;
Tebib, N. ;
Azzouz, H. ;
Abdelmoula, M. Slim ;
Ben Chehida, A. ;
Hubert, P. ;
Douira, W. ;
Ben Dridi, M. F. .
ARCHIVES DE PEDIATRIE, 2009, 16 (01) :27-31
[8]   AN UNDIAGNOSED ENDOCRINOMETABOLIC SYNDROME - REPORT OF 2 CASES [J].
BERARDINELLI, W .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1954, 14 (02) :193-204
[9]   Cardiomyopathy in congenital complete lipodystrophy [J].
Bhayana, S ;
Siu, VM ;
Joubert, GI ;
Clarson, CL ;
Cao, H ;
Hegele, RA .
CLINICAL GENETICS, 2002, 61 (04) :283-287
[10]   Seipin deficiency alters fatty acid Δ9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy [J].
Boutet, Emilie ;
El Mourabit, Haquima ;
Prot, Matthieu ;
Nemani, Mona ;
Khallouf, Eliane ;
Colard, Odile ;
Maurice, Michele ;
Durand-Schneider, Anne-Marie ;
Chretien, Yves ;
Gres, Sandra ;
Wolf, Claude ;
Saulnier-Blache, Jean-Sebastien ;
Capeaua, Jacqueline ;
Magre, Jocelyne .
BIOCHIMIE, 2009, 91 (06) :796-803