TWO SYNDROMES IN THE SAME FAMILY TREE: DOWN AND PRADER-WILLI-LABHART SYNDROMES

M. Bogavac ,
M. Bogavac

Clinical Center Novi Sad, Department of Obstetrics and Gynecology , Novi Sad , Serbia

G. Relić ,
G. Relić

Clinical Center Novi Sad, Department of Obstetrics and Gynecology , Novi Sad , Serbia

A. Mitreski ,
A. Mitreski

Unit of Obstetrics and Gynecology “Minerva” , Novi Sad , Serbia

D. Katanić ,
D. Katanić

Institute of the Young Children and Youth Health Care in Novi Sad , Novi Sad , Serbia

J. Jovanović-Privrodski
J. Jovanović-Privrodski

Institute of the Young Children and Youth Health Care in Novi Sad , Novi Sad , Serbia

Published: 01.12.2004.

Volume 32, Issue 2 (2004)

pp. 85-88;

https://doi.org/10.70949/pramed200402098B

Abstract

The genes mutate either spontaneously or under the influence of mutagenic agents (irradiation, viruses, toxins).
The occurrence of genetic syndromes in the scope of one family is pointing more to the inherited than to de novo mutation.
Aim of this study was to present two syndromes in the same family tree, occurring subsequently one by one, which carry severe mental retardation and have a poor prognosis and frequently tragic outcome. A case report was given of a patient in
whom both pregnancies were completed by birth of the newborns presenting with severe syndromes: the first one with
Down's syndrome and the second one with Prader-Willi-Labhart syndrome. The results of investigation point to the necessity of genetic investigations before pregnancy and during pregnancy as early as possible, in order to avoid giving birth to
the children with syndromes which bear severe mental retardation and having poor prognosis.

Keywords

References

1.
Reynolds TM. Down’s syndrome screening: a controversial test, with more controversy to come! J Clin Pathol. Dec;53(12):893-8.
2.
Sagot P. Controversy: systemic amniocentesis for women 38 years and more? Gynecol Obstet Fertil. Oct;28(10):769-71.
3.
Gardiner K, Davisson M. The sequence of human chromosome 21 and implications for research into Down syndrome. Genome Biol. 1(2).
4.
5.
Eiholzer U, Bachmann S, l’Allemand D. Is there growth hormone deficiency in Prader-Willi Syndrome? Horm-Res. 3:44–52.
6.
Schmeling H, Gillessen-Kaesbach G, Schulte-Mattler U, Burdach S, Horneff G. Prader-Labhart-Willi syndrome in infants. Klin Padiatr. 214(2):51–3.
7.
Kobayashi N, Komiyama A. Down’s syndrome. Ryoikibetsu Shokogun Shirizu. 32:279–81.
8.
Cheffins T, Chan A, Haan EA, Ranieri E, Ryall RG, Keane RJ, et al. The impact of maternal serum screening on the birth prevalence of Down’s syndrome and the use of amniocentesis and chorionic villus sampling in South Australia. BJOG. Dec;107(12):1453-9.
9.
Onda T, Tanaka T, Yoshida K. Triple marker screening for trisomy 21, trisomy 18 and open neural tube defects in singleton pregnancies of native Japanese pregnant women. J Obstet Gynaecol Res. 26(6):441–7.
10.
Poon LL, Leung TN, Lau TK, Lo YM. Prenatal detection of fetal Down’s syndrome from maternal plasma. Lancet. 14;356(9244):1819-20.
11.
Wallace AM, Hunter I, Galloway P, Greene SA, Donaldson MD. Obesity in the Prader-Labhart-Willi syndrome is not due to leptin deficiency but is accentuated by hypogonadism in male patients. Clin Endocrinol (Oxf. Dec;51(6):816-7.
12.
Eiholzer U, l’Allemand D. Growth hormone normalises height, prediction of final height and hand length in children with Prader-Willi syndrome after 4 years of therapy. Horm-Res. 53(4):185–92.
13.
Schulze A, Mogensen H, Hamborg-Petersen B, Græm N, Osgelton BN, K. Fertility in Prader-Willi syndrome: a case report with Angelman syndrome in the offspring. Acta Pæd Scand.

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