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Relevant bibliographies by topics / Mermaid baby syndrome

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Journal articles

Academic literature on the topic 'Mermaid baby syndrome'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Mermaid baby syndrome"

1

Siddique, Md Abu Bakkar, Sudip Saha, Kallol Bose, Sudipta Ghorai, and Kalimuddin Khan. "Mermaid Syndrome." Journal of Nepal Paediatric Society 38, no. 2 (2019): 132–34. http://dx.doi.org/10.3126/jnps.v38i2.18802.

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We report a case of sirenomelia baby (Mermaid syndrome) born to a twenty three years old female at 37 weeks of gestation. Sirenomelia is characterized by fusion of the lower limbs with absent kidneys, absent external genitalia and other gastrointestinal defects. It results from the failure of normal vascular supply from the lower aorta in vitro, maternal Diabetes mellitus has been associated with caudal regression syndrome and sirenomelia.

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2

Defrin, Defrin, Calvindra Leenesa, and Marcella Marcella. "Sirenomelia (Mermaid Syndrome)." Indonesian Journal of Obstetrics & Gynecology Science 4, no. 2 (2021): 185–91. http://dx.doi.org/10.24198/obgynia.v4n2.243.

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Abstract Objective: To report a rare fetal abnormalities case Method: Case report Case: Reported case of a 37-year-old patient came to the emergency room at RSIA Siti Hawa Padang with complaints of inpartu signs in the last 8 hours before entering the hospital. After the examination, the diagnosis was G3P2A0L3 35-36 weeks of preterm parturient active phase of first stage + twice previous CS + breech presentation. Then, the patient was planned for an emergency CS at 07.50 am. Born babies with genitalia form was not identified, BW: 2030 grams, BH: 30 cm, Scoring Apgar: 3/5, there are congenital

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3

Sandhu, AvneetSingh, Gyan Ranjan, Shashank Singh, and Santosh Kumar. "MERMAID BABY SYNDROME WITH GENU RECURVATUM." International Journal of Advanced Research 5, no. 5 (2017): 538–39. http://dx.doi.org/10.21474/ijar01/4142.

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4

Trivedi, Swati, Oby Nagar, J. P. Soni, Shashank Trivedi, and Prasoon Rastogi. "A case report of sirenomelia with two umbilical arteries: an unusual finding in a rare case." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 10, no. 9 (2021): 3640. http://dx.doi.org/10.18203/2320-1770.ijrcog20213505.

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Sirenomelia also known as Mermaid syndrome is a rarely encountered fusion anomaly of the caudal region of body often associated with Potter’s facies, single umbilical artery and various visceral abnormalities which make it irreconcilable with life. Here we report a case of sirenomelia delivered in our tertiary care hospital by lower segment cesarean section to a 24 year old third gravida with no previous live issues. No high risk factors could be identified with the mother including diabetes mellitus. Baby was born alive with Potter’s facies. Both the lower limbs were merging into each other l

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5

Defrin, Defrin, Calvindra Leenesa, and Marcella Marcella. "Sirenomelia (Mermaid Syndrome)." Indonesian Journal of Obstetrics & Gynecology Science 4, no. 2 (2021): 185. http://dx.doi.org/10.24198/obgynia.v4i2.243.

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Objective: To report a rare fetal abnormalities caseMethod: Case reportCase: Reported case of a 37-year-old patient came to the emergency room at RSIA Siti Hawa Padang with complaints of inpartu signs in the last 8 hours before entering the hospital. After the examination, the diagnosis was G3P2A0L3 35-36 weeks of preterm parturient active phase of first stage + twice previous CS + breech presentation. Then, the patient was planned for an emergency CS at 07.50 am. Born babies with genitalia form was not identified, BW: 2030 grams, BH: 30 cm, Scoring Apgar: 3/5, there are congenital abnormaliti

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6

Riazat, Muhammad Imran, Bharti Kewlani, Jamaleddin Abujennah, and Farhana Sharif. "Sirenomelia (mermaid syndrome): a rare congenital disorder." BMJ Case Reports 12, no. 11 (2019): e229970. http://dx.doi.org/10.1136/bcr-2019-229970.

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Sirenomelia, also known as mermaid syndrome, is an extremely rare congenital disorder involving the lower spine and lower limbs. We present a case of a grand multiparous with poorly controlled gestational diabetes who delivered a live baby weighing 2.43 kg at 38 weeks’ gestation. The baby was noted to have significant respiratory distress, and resuscitation was promptly commenced. Severe congenital abnormalities indicative of sirenomelia were obvious and after availability of antenatal records which indicated an extremely poor prognosis, resuscitative efforts were aborted. The baby was handed

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7

Bhattacherjee A, Haque R, Shahabuddin M, Noor ZB, Akhter P, and Samad A. "Mermaid baby: Fairy tale in practical." Journal of Sylhet Women’s Medical College 14, Number 1 (2024): 84–86. http://dx.doi.org/10.47648/jswmc2024v14-01-18.

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Sirenomelia, also called Mermaid syndrome is a rare and fatal anomaly which is characterized by a single lower extremity featuring a Mermaid like appearance where head and trunk is like humans and lower extremity is like tail of a fish. It is associated with other gastro-intestinal, genito-urinary and other organ abnormalities. Most patients die shortly after birth. The exact cause of Sirenomelia is unknown. Here we present a newborn baby with Sirenomelia. Mother had bad obstetric history, antenatal ultrasonography revealed severe oligohydramnios and renal agenesis. On examination there was dy

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8

Ram Jeewan Singh, Bijay Kumar Suman, Keerthana Bachala, Amit Kumar, Rashi Rashi, and Amit Kumar Sinha. "Mermaid baby or sirenomelia: a lethal congenital anomaly." International Journal of Contemporary Pediatrics 10, no. 5 (2023): 736–37. http://dx.doi.org/10.18203/2349-3291.ijcp20231152.

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Mermaid syndrome is a very rare, lethal congenital anomaly. It is associated with other congenital anomalies and is incompatible with life. Typical clinical features are fused lower limb from perineum to ankle and single umbilical artery. Etiology is multifactorial and is extreme form of caudal regression syndrome. When diagnosed in early gestation, termination of pregnancy may be considered.

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9

Joshi, Reetika, Veino Kuveio Duomai, and Bianchi Sangma. "Sirenomelia, the mermaid baby: a case report." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 11 (2019): 4609. http://dx.doi.org/10.18203/2320-1770.ijrcog20194907.

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Sirenomelia sequence or mermaid syndrome is a rare congenital structural anomaly characterized by different degrees of fusion of lower limbs, thoracolumbar spinal anomalies, sacrococcygeal agenesis, genitourinary and anorectal atresia. The incidence of sirenomelia is 0.8-1 cases/ 105 births with male to female ratio being 3:1. A malformations patient with 40 weeks of gestation admitted with complaints of decreased fetal movements for one week. An emergency C-section was done in view of term pregnancy with severe oligohydramnios and intrauterine growth restriction with poor bishop’s score. A 1.

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10

Siddiqua, Sehereen Farhad, Sharmin Abbasi, and Abrar Saqif Hasan. "Sirenomelia: The Mermaid Syndrome-A Rare Case Report." Anwer Khan Modern Medical College Journal 8, no. 2 (2017): 144–47. http://dx.doi.org/10.3329/akmmcj.v8i2.33672.

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Sirenomelia, which is also known as mermaid syndrome, is an extremely rare congenital developmental disorder characterized by anomalies of the lower spine and the lower limbs. Affected infants are born with partial or complete fusion of the legs1. Additional malformations may also occur including genitourinary abnormalities, gastrointestinal abnormalities, anomalies of the lumbarsacral spine and pelvis and absence or underdevelopment (agenesis) of one or both kidneys. Affected infants may have one foot, no feet or both feet, which may be rotated externally. The tailbone is usually absent and t

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