Fol. Biol. 2019, 65, 134-141
https://doi.org/10.14712/fb2019065030134
Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case
References
1. , L., Hertecant, J., Algawi, K., El Teraifi, H., Dattani, M. (2008) A new autosomal recessive syndrome of ocular colobomas, ichthyosis, brain malformations and endocrine abnormalities in an inbred Emirati family. Am. J. Med. Genet. A 146A, 813-819.
<https://doi.org/10.1002/ajmg.a.32114>
2. , Y., Ben-Omran, T., Tolefat, M., Bejaoui, Y., El-Shanti, H., Kambouris, M. (2014) A novel missense mutation in SRD5A3 causes congenital disorder of glycosylation type I (Cerebello-Ocular Syndrome). J. Inborn Errors Metab. Screen. 2, 3-7.
<https://doi.org/10.1177/2326409814550528>
3. , B., Hackler, R., Peters, V., Schaefer, J. R., Arndt, T., Mayatepek, E., Jaeken, J., Hoffmann, G. F. (2001) A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestations. Neuropediatrics 32, 313-318.
<https://doi.org/10.1055/s-2001-20407>
4. , V., Lefeber, D. J., Ng, B. G., Guan, Z., Silhavy, J. L., Bielas, S. L., Lehle, L., Hombauer, H., Adamowicz, M., Swiezewska, E., De Brouwer, A. P., Blümel, P., Sykut-Cegielska, J., Houliston, S., Swistun, D., Ali, B. R., Dobyns, W. B., Babovic-Vuksanovic, D., van Bokhoven, H., Wevers, R. A., Raetz, C. R., Freeze, H. H., Morava, E., Al-Gazali, L., Gleeson, J. G. (2010) SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder. Cell 142, 203-217.
<https://doi.org/10.1016/j.cell.2010.06.001>
5. , J. E., Guan, Z., Rust, S., Reunert, J., Müller, B., Du Chesne, I., Zerres, K., Rudnik-Schöneborn, S., Ortiz- Brüchle, N., Häusler. M. G., Siedlecka, J., Swiezewska, E., Raetz, C. R., Marquardt, T. (2012) Life with too much polyprenol: polyprenol reductase deficiency. Mol. Genet. Metab. 105, 642-651.
<https://doi.org/10.1016/j.ymgme.2011.12.017>
6. , M., Wada, Y., Hansikova, H., Yuasa, I., Vesela, K., Ondruskova, N., Kadoya, M., Janssen, A., Van den Heuvel, L. P., Morava, E., Zeman, J., Wevers, R. A., Lefeber, D. J. (2011) Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I. J. Inherit. Metab. Dis. 34, 901-906.
<https://doi.org/10.1007/s10545-011-9311-y>
7. , N., Verma, G., Kabra, M., Bijarnia-Mahay, S., Ganapathy, A. (2018) Identification of a case of SRD5A3 – congenital disorder of glycosylation (CDG1Q) by exome sequencing. Indian J. Med. Res. 147, 422-426.
<https://doi.org/10.4103/ijmr.IJMR_820_16>
8. , J., van Eijk, H. G., van der Heul, C., Corbeel, L., Eeckels, R., Eggermont, E. (1984) Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome. Clin. Chim. Acta 144, 245-247.
<https://doi.org/10.1016/0009-8981(84)90059-7>
9. , K., Najmabadi, H., Kariminejad, R., Jamali, P., Malekpour, M., Garshasbi, M., Ropers, H. H., Kuss, A. W., Tzschach, A. (2009) An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4. Eur. J. Hum. Genet. 1, 125-128.
<https://doi.org/10.1038/ejhg.2008.159>
10. , K., Hu, C. H., Garshasbi, M., Abedini, S. S., Ghadami, S., Kariminejad, R., Ullmann, R., Chen, W., Ropers, H. H., Kuss, A. W., Najmabadi, H., Tzschach, A. (2011) Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3. Eur. J. Hum. Genet. 19, 115-117.
<https://doi.org/10.1038/ejhg.2010.132>
11. , B., Ayhan, Ö., Gökçay, G., Başboğaoğlu, N., Tolun, A. (2014) Adult phenotype and further phenotypic variability in SRD5A3-CDG. BMC Med. Genet. 15, 10.
<https://doi.org/10.1186/1471-2350-15-10>
12. , C. S., Tümer, L., Ezgü, F. S., Hasanoğlu, A., Race, V., Matthijs, G., Jaeken, J. (2012) SRD5A3-CDG: a patient with a novel mutation. Eur. J. Paediatr. Neurol. 16, 554-556.
<https://doi.org/10.1016/j.ejpn.2011.12.011>
13. , A. O. (2018) Early-onset retinal dystrophy and chronic dermatitis in a girl with an undiagnosed congenital disorder of glycosylation (SRD5A3-CDG). Ophthalmic Genet. 39, 628-630.
<https://doi.org/10.1080/13816810.2018.1498529>
14. , E., Wosik, H. N., Sykut-Cegielska, J., Adamowicz, M., Guillard, M., Wevers, R. A., Lefeber, D. J., Cruysberg, J. R. (2009) Ophthalmological abnormalities in children with congenital disorders of glycosylation type I. Br. J. Ophthalmol. 93, 350-354.
<https://doi.org/10.1136/bjo.2008.145359>
15. , E., Wevers, R. A., Cantagrel, V., Hoefsloot, L. H., Al-Gazali, L., Schoots, J., van Rooij, A., Huijben, K., van Ravenswaaij-Arts, C. M., Jongmans, M. C., Sykut-Cegielska, J., Hoffmann, G. F., Bluemel, P., Adamowicz, M., van Reeuwijk, J., Ng, B. G., Bergman, J. E., van Bokhoven, H., Körner, C., Babovic-Vuksanovic, D., Willemsen, M. A., Gleeson, J. G., Lehle, L., de Brouwer, A. P., Lefeber, D. J. (2010) A novel cerebello-ocular syndrome with abnormal glycosylation due to abnormalities in dolichol metabolism. Brain 133, 3210-3220.
<https://doi.org/10.1093/brain/awq261>
16. , V., Peters, V., Hackler, R., Jakobi, R., Assmann, B., Fang, J., Körner, C., Helwig-Rolig, A., Schaefer, J. R., Hoffmann, G. F. (2002) A new case of CDG-x with stereotyped dystonic hand movements and optic atrophy. J. Inherit. Metab. Dis. 25, 126-130.
<https://doi.org/10.1023/A:1015628810892>
17. , R. L., Arno, G., Poulter, J. A., Khan, K. N., Morarji, J., Hull, S., Pontikos, N., Rueda Martin, A., Smith, K. R., Ali, M., Toomes, C., McKibbin, M., Clayton-Smith, J., Grunewald, S., Michaelides, M., Moore, A. T., Hardcastle, A. J., Inglehearn, C. F., Webster, A. R., Black, G. C., UK Inherited Retinal Disease Consortium and the 100,000 Genomes Project. (2017) Association of steroid 5α-reductase type 3 congenital disorder of glycosylation with early-onset retinal dystrophy. JAMA Ophthalmol. 135, 339-347.
<https://doi.org/10.1001/jamaophthalmol.2017.0046>
18. , B., Pehlivan, D., Özkök, A., Jhangiani, S., Yalcinkaya, C., Zeybek, Ç. A., Muzny, D. M., Lupski, J. R., Gibbs, R., Jaeken, J. (2016) Phenotypic expansion of congenital disorder of glycosylation due to SRD5A3 null mutation. JIMD Rep. 26, 7-12.
<https://doi.org/10.1007/8904_2015_478>
19. , P. G., Ng, B. G., Sanford, L., Sutton, V. R., Bartholomew, D. W., Pastore, M. T., Bamshad, M. J., Kircher, M., Buckingham, K. J., Nickerson, D. A., Shendure, J., Freeze, H. H. (2016) SRD5A3-CDG: expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features. Am. J. Med. Genet. A 170, 3165-3171.
<https://doi.org/10.1002/ajmg.a.37875>
