Trisomy 18 (Edwards Syndrome) was first reported in 1960 by Edward et al. in a newborn with multiple abnormalities, and is a broad clinical presentation involving more than 130 different abnormalities. Most cases die during the embryonic or fetal life. Only 5% - 10% of the live-born cases survive the first year of life. Prenatal diagnosis is possible. However, the prenatal detection compels parents to make a difficult decision. After the birth of the baby, it also places a material and moral burden on both the family and the national economy due to multiple congenital abnormalities and limited lifespan. On the other hand, pediatricians experience difficulties in making a decision on interventions, especially cardiac surgery and resuscitation, due to the comorbid abnormalities in the neonatal intensive care units, in which medical ethics arises for discussion. The current study presents a case diagnosed with trisomy 18 by chromosome analysis, who was found to have multiple abnormalities with ultrasonography (USG) during the prenatal period and born because the patient’s mother, who was advised to have amniocentesis, decided to continue with the pregnancy.
Trisomy 18 was first described in 1960 by Edward et al. in a newborn with multiple abnormalities and cognitive deficiency. Later in the same year, Smith et al. demonstrated additional chromosomes to the 18th chromosome. Initially known as trisomy 17 - 18 (new trisomy), this syndrome is the second most common syndrome after Down syndrome, among autosomal trisomies [
Most cases die during the embryonic or fetal life. The average lifespan is 2.5 - 14.5 days. Prenatal diagnosis is possible. However, the prenatal detection compels parents to make a difficult decision.
The current study presents a case diagnosed with trisomy 18 by chromosome analysis, who was found to have multiple abnormalities with USG during the prenatal period and born because the patient’s mother, who was advised to have amniocentesis, decided to continue with the pregnancy.
The patient born as a 37-week baby girl via cesarean delivery from the third pregnancy of a 36-year-old mother was transferred to the neonatal intensive care unit due to respiratory distress. The mother had a history of using antibiotics during her pregnancy due to a urinary tract infection and tooth infection. The mother had been advised at her pregnancy follow-ups to have amniocentesis because of microcephaly and intrauterine growth retardation, but the family did not accept this procedure. At the physical examination, the weight was 1740 g (<3% percentile), head circumference was 30 cm (<3% percentile), and height was 39 cm (<3% percentile). There were bilateral low-set ears, micrognathia, short neck, flexion of the fingers of both hands and finger overlaps, outwardly prominent heels, and clitoromegaly (Figures 1-3). Gluteal muscles were atrophic. At the cardiac ex-
amination, KTA: 120/min sulf was not heard. Due to multiple abnormalities, echocardiography (ECHO) was requested. The laboratory examination revealed normal whole blood count, and kidney and liver function tests. Vitamin D levels were studied in the biochemistry tests due to hypocalcemia. The level of 25-(OH)-vitamin D was 15.98 nmol/L. Chromosome analysis revealed 47 XX + 18. Abdominal USG was considered normal. The ECHO assessment revealed patent ductus, bicuspid aorta, pulmonary hypertension, and ventricular septal defect (VSD).
The patient who was transferred to the neonatal intensive care unit due to respiratory distress was administered nasal CPAP + IV fluid + antibiotic + vitamin D deficiency treatment. She was followed-up by administering O2 with CPAP for 13 days and hood for ten days. She was discharged on day 42. She was hospitalized three more times due to bronchopneumonia one week after the discharge. The patient, who is 7.5 months old now, is still being followed-up at the polyclinic.
Trisomy 18 is a syndrome with a very limited prognosis, involving more than 130 different abnormalities in the literature and affecting almost all organs and systems, none of which are pathognomonic [
Prenatal diagnosis is possible through cytogenetic examination requested in the presence of pathologies such as increased neck skin thickness, intrauterine growth retardation, polyhydramnios, bilateral choroid plexus cyst, and cardiac abnormalities at the prenatal (USG) examination [
Our patient, as reported in the literature, was a 37-week preterm, had low birth weight, born via cesarean delivery, and had low Apgar score (6 at minute 1 and 7 at minute 5).
In trisomy 18 babies, intrauterine growth retardation; micrognathia, microcephaly; low-set ears; gastrointestinal and extremity abnormalities; mental retardation; ocular abnormalities such as glaucoma, microphthalmia and cataract; clitoromegaly; and congenital cardiac abnormalities are common. The appearance of overlapping fingers is typical. The most common congenital abnormalities are VSD, atrial septal defect (ASD), patent ductus arteriosus (PDA), and pulmonary hypertension [
The survival rate of trisomy 18 cases depends on comorbid abnormalities. The average lifespan is 1.5 - 14.5 days and 95% of the pregnancies result in embryonic or fetal deaths, whereas only 5% - 10% of the live-born cases survive the first year of life. The literature reports the most common causes of mortality as congenital heart diseases, aspiration pneumonia, sepsis, and renal failure [
In conclusion, the combined effects of both genetics and environment are responsible for the etiology of trisomy 18. Prenatal diagnosis is possible. However, the prenatal detection compels parents to make a difficult decision. Therefore, importance is likely to be placed on clarifying and managing etiological factors in future clinical studies.
There isn’t any financial disclosure.
The authors declare that they have no conflict of interest.
AtiyeFedakâr,SevalEren,Elif ÖzbeyAkan,SelahattinSemiz, (2016) Trisomy 18: A Difficult Decision for the Family. Open Journal of Pediatrics,06,136-140. doi: 10.4236/ojped.2016.61020