Nail-patella syndrome (NPS), also known as hereditary onycho-osteodystrophy (HOOD) is a rare inherited autosomal dominant disease with involvement of the LMX1 gene. We report a case of NPS with atypical involvement of the lip, palate, and lung and discuss the possible genetic associations between NPS, recurrent pneumothoraces, and cleft lip/palate.
BongersEMKnoersNC. From gene to disease; the nail-patella syndrome and the LMX1 gene. Ned Tijdschr Geneeskd2003;147:67–9.
2.
McIntoshIDunstonJALiuLHoover-FongJESweeneyE. Nail patella syndrome revisited: 50 years after linkage. Ann Hum Genet2005;69:349–63.
3.
MorelloRZhouGDreyerSDHarveySJNinomiyaYThornerPS. Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome. Nat Genet2001; 27:205–8.
4.
LemleyKV. Kidney disease in nail-patella syndrome. Pediatr Nephrol2009;24;2345–54.
5.
SweeneyEFryerAMountfordRGreenAMcIntoshI. Nail patella syndrome: A review of the phenotype aided by developmental biology. J Med Genet2003;40:153–162.
6.
LucasGLOpitzJMWifflerC. The nail patella syndrome. Clinical and genetic aspects of 5 kindreds with 38 affected family members. J Pediatr1996;68:273–88.
7.
LooijBJJrte SlaaRLHogewindBLvan de KampJJ. Genetic counseling in hereditary osteo-onychodysplasia (HOOD, nail-patella syndrome) with nephropathy. J Med Genet1988;25:682–6.
8.
MeyrieARizzoRGublerMC. The nail-patella syndrome. A review. J Nephrol1990;2:133–40.
9.
Richieri-CostaA. Antecubital pterygium and cleft lip/palate presenting as signs of the nail-patella syndrome: Report of a Brazilian family. Am J Med Genet1991; 38:9–12.
10.
LidralACMurrayJCBuetowKHBasartAMSchearerHShiangR. Studies of the candidate genes TGFB2, MSX 1, TGFA, and TGFB3 in the etiology of cleft lip and palate in Philippines. Cleft Palate Craniofac J1997;34:1–6.
11.
LidralACRomittiPABasartAMDoetschmanTLeysensNJDaack-HirschS. Association of MSX 1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet1998;63:557–68.
12.
SarapuraVDStrouthHLGordonDFWoodWMRidgwayEC. Msx1 is present in thyrotropic cells and binds to a consensus site on the glycoprotein hormone alpha-subunit promoter. Mol Endocrinol1997;11:1782–94.
13.
van den BoogaardMJDorlandMBeemerFAvan AmstelHK. MSX 1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet2000;24:342–3.
14.
KrapelsIPVermeij-KeersCMullerMde KleinASteegers-TheunissenRP. Nutrition and genes in the development of orofacial clefting. Nutr Rev2006;64:280–8.
15.
KaartinenVVonckenJWShulerCWarburtonDBuDHeisterkampN. Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction. Nat Genet1995;11:415–21.
16.
ShiWHeisterkampNGroffenJZhaoJWarburtonDKaartinenV. TGF-beta3-null mutation does not abrogate fetal lung maturation in vivo by glucocorticoids. Am J Physiol1999;277:L1205–13.