Abstract
We report the first case of maternal uniparental disomy for chromosome 6 (UPD6mat) ascertained through congenital adrenal hyperplasia (CAH), which arose because of reduction to homozygosity of an autosomal recessive mutation. This case suggests that UPD6mat is associated with intrauterine growth retardation (IUGR). A case of paternal UPD (involving only the short arm of chromosome 6) ascertained as CAH has previously been reported, but was not stated to have IUGR. Our patient was born with IUGR followed by extraordinarily good catch-up growth. She had a history of a marked lag in motor development. She presented at 2.65 y of age with pubarche of 3 mo duration, clitoral enlargement, and an advanced bone age. Simple virilizing CAH was diagnosed by elevations of plasma 17-hydroxyprogesterone and testosterone. Mutation analysis showed that the CAH was due to homozygosity for the I172N exon 4 mutation. When parental DNA was examined, the mother was found to be heterozygous for the uncommon exon 4 mutation, while the father had no detectable mutations. DNA microsatellite analysis was subsequently performed on the patient and parents using polymorphic markers spanning the entire chromosome 6. Seven markers were informative for inheritance of a single maternal allele and absence of paternal alleles in the proband. Analysis of microsatellite markers from other chromosomes confirmed biparental inheritance at these loci. This combination of findings is diagnostic of UPD6mat. The only other reported case of UPD6mat was discovered serendipitously when genotyped for renal transplantation; this patient had a history of IUGR. Since both cases of UPD6mat had IUGR, the phenotype appears to include IUGR as well as the potential to unmask an autosomal recessive trait.
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Abbreviations
- CAH:
-
congenital adrenal hyperplasia
- CYP21:
-
cytochrome P450c21
- IUGR:
-
intrauterine growth retardation
- UPD:
-
uniparental disomy
- UPD6mat:
-
uniparental disomy of chromosome 6 (maternal)
References
New M 1995 Steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia). Am J Med 98: 2S–8S
White PC, Tusie-Luna MT, New MI 1994 Mutations in steroid 21-hydroxylase (CYP21). Human Mutat 3: 373–378
Wedell A 1998 Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): implications for diagnosis, prognosis and treatment. Acta Paediatr 87: 159–164
Wedell A, Thilen A, Ritzen EM, Stengler B, Luthman H 1994 Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation. J Clin Endocrinol Metab 78: 1145–1152
Wilson R, Mercado A, Cheng K, New M 1995 Steroid 21-hydroxylase deficiency: genotype may not predict phenotype. J Clin Endocrinol Metab 80: 2322–2329
Mornet E, Crete P, Kuttenn F, Raux-Demay MC, Boue J, White PC, Boue A 1991 Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency. Am J Human Genet 48: 79–88
Wilson RC, Wei JQ, Cheng KC, Mercado AB, New MI 1995 Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene. J Clin Endocrinol Metab 80: 1635–1640
White PC, Vitek A, Dupont B, New MI 1988 Characterization of frequent deletions causing steroid 21-hydroxylase deficiency. Proc Natl Acad Sci U S A 85: 4436–4440
Christian SL, Rich BH, Loebl C, Israel J, Vasa R, Kittikamron K, Spiro R, Rosenfield R, Ledbetter DH 1999 Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus. J Pediatr 134: 42–46
Engel E 1998 Uniparental disomies in unselected populations. Am J Hum Genet 63: 962–966
Bartolomei MS, Tilghman SM 1997 Genomic imprinting in mammals. Annu Rev Genet 31: 493–525
Shaffer LG, McCaskill C, Adkins K, Hassold TJ 1998 Systematic search for uniparental disomy in early fetal losses: the results and a review of the literature [In Process Citation]. Am J Med Genet 79: 366–372
Morison IM, Reeve AE 1998 A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Hum Mol Genet 7: 1599–1609
Mutter GL 1997 Role of imprinting in abnormal human development. Mutat Res 396: 141–147
Cassidy SB 1995 Uniparental disomy and genomic imprinting as causes of human genetic disease. Environ Mol Mutagen 25: 13–20
Spence JE, Perciaccante RG, Greig GM, Willard HM, Ledbetter DH, Hejmancik JF, Pollack MS, O'Brien WE, Beaudet AL 1988 Uniparental disomy as a mechanism for human disease. Am J Human Genet 42: 217–226
Voss R, Ben-Simon E, Avital A, Godfrey S, Zlotogora J, Dagan J, Tikochinski Y, Hillel J 1989 Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?. Am J Human Genet 45: 373–380
Quan F, Janas J, Toth-Fejel S, Johnson DB, Wolford JK, Popovich BW 1997 Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy. Am J Human Genet 60: 160–165
van den Berg-Loonen EM, Savelkoul P, van Hooff H, van Eede P, Riesewijk A, Geraedts J 1996 Uniparental maternal disomy 6 in a renal transplant patient. Human Immunol 45: 46–51
Temple IK, Gardner RJ, Robinson DO, Kibirige MS, Ferguson AW, Baum JD 1996 Further evidence for an imprinted gene for neonatal diabetes localized to chromosome 6q22–q23. Human Mol Genet 8: 117–121
Hermann R, Soltész G 1997 Paternal uniparental isodisomy of chromosome 6 in transient neonatal diabetes mellitus (letter). Eur J Pediatr 156: 740
Whiteford ML, Narendra A, White MP, Cooke A, Wilkinson AG, Robertson KJ, Tolmie JL 1997 Paternal uniparental disomy for chromosome 6 causes transient neonatal diabetes. J Med Genet 34: 167–168
Menon RK, Sperling MA 1996 Insulin as a growth factor. Endocrinol Metab Clin North Am 25: 633–647
Lopez-Gutierrez AU, Riba L, Ordonez-Sanchez ML, Ramirez-Jimenez S, Cerrillo-Hinojosa M, Tusie-Luna MT 1998 Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease [In Process Citation]. J Med Genet 35: 1014–1019
Thilen A, Woods KA, Perry LA, Savage MO, Wedell A, Ritzen EM 1995 Early growth is not increased in untreated moderately severe 21-hydroxylase deficiency [see comments]. Acta Paediatr 84: 894–898
Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH 1993 Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11–q13): molecular diagnosis and mechanism of uniparental disomy. Hum Mol Genet 2: 143–151
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Editorial assistance was provided by Jean Moore.
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Supported in part by USPHS-RR-00055 (R.L.R), RR-06020, and HD-00072 (M.I.N.).
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Spiro, R., Christian, S., Ledbetter, D. et al. Intrauterine Growth Retardation Associated with Maternal Uniparental Disomy for Chromosome 6 Unmasked by Congenital Adrenal Hyperplasia. Pediatr Res 46, 510 (1999). https://doi.org/10.1203/00006450-199911000-00004
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DOI: https://doi.org/10.1203/00006450-199911000-00004
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