MIKROMELIA IN NEWBORNS: MIDWIFERY MANAGEMENT AND CLINICAL IMPLICATIONS

Authors

  • Yosefin Nainggolan Sekolah Tinggi Ilmu Kesehatan Mitra Husada Medan
  • Tina Sekolah Tinggi Ilmu Kesehatan Mitra Husada Medan
  • Ernawati Nasution Sekolah Tinggi Ilmu Kesehatan Mitra Husada Medan
  • Agusmawati Zega Sekolah Tinggi Ilmu Kesehatan Mitra Husada Medan
  • Nazibah Saridatun Nahla Sekolah Tinggi Ilmu Kesehatan Mitra Husada Medan

Keywords:

Micromelia, Congenital Anomaly, Skeletal Dysplasia, Midwifery Care, Newborn

Abstract

Background: Micromelia is a rare congenital skeletal dysplasia characterized by generalized shortening of the upper and lower extremities due to impaired endochondral ossification during fetal development. Early detection and appropriate management are essential to reduce complications and improve neonatal outcomes. Objectives: This study aimed to describe the concept of micromelia and analyze the implementation of midwifery care management in infants diagnosed with this congenital anomaly. Methods: This study employed a descriptive case study approach based on literature review and application of Varney’s seven-step midwifery management process. Data were collected through assessment, physical examination, identification of problems and needs, planning, implementation, and evaluation of care in an infant with micromelia. Results: The case assessment revealed generalized shortening of the upper and lower extremities, mild respiratory distress, weak sucking reflex, and risk of growth and developmental problems. Midwifery management included monitoring vital signs, maintaining body temperature, supporting breastfeeding, observing respiratory function, providing parental education, and collaborating with pediatric specialists for further evaluation and referral. The infant's condition remained stable, and the family demonstrated improved understanding of the condition and agreed to the referral plan. Conclusions: Comprehensive and evidence-based midwifery care plays an important role in the early detection, monitoring, referral, and family support of infants with micromelia. Multidisciplinary collaboration is essential to optimize clinical outcomes and improve the quality of life of affected infants.

References

American Academy of Pediatrics. Guidelines for Neonatal Assessment and Management of Congenital Anomalie (2024). Pediatrics, 154, e20240678.

American College of Obstetricians and Gynecologists. Screening and Diagnostic Testing for Genetic Disorders During Pregnancy (2024). Obstetrics & Gynecology, 143, e1–e18.

Crane, H. M., Schindewolf, E., Burrill, N., et al. The Reliability of Ultrasound Markers in Identifying Fetuses With a Life-Limiting Skeletal Dysplasia (2024). Prenatal Diagnosis, 44, 1318–1326. https://doi.org/10.1002/pd.6638

Indonesian Midwives Association. Evidence-Based Midwifery Practice in Maternal and Neonatal Care (2023). Jakarta: IBI Press.

International Federation of Gynecology and Obstetrics. FIGO Good Clinical Practice Advice on Prenatal Diagnosis of Congenital Anomalies (2024). International Journal of Gynecology and Obstetrics, 166, 15–27.

International Society of Ultrasound in Obstetrics and Gynecology (ISUOG). Practice Guidelines: Performance of the Routine Mid-Trimester Fetal Ultrasound Scan (2024). Ultrasound in Obstetrics & Gynecology, 63, 111–128.

Kementerian Kesehatan Republik Indonesia. Pedoman Pelayanan Antenatal Terpadu Edisi Terbaru (2023). Jakarta: Kementerian Kesehatan RI.

Kementerian Kesehatan Republik Indonesia. Pedoman Pelayanan Neonatal Esensial (2023). Jakarta: Kementerian Kesehatan RI.

Kementerian Kesehatan Republik Indonesia. Profil Kesehatan Indonesia Tahun 2024 (2025). Jakarta: Kementerian Kesehatan RI.

Kline-Fath, B. M. Fetal Skeletal Dysplasia. (2024). Magnetic Resonance Imaging Clinics of North America, 32, 497–511. https://doi.org/10.1016/j.mric.2024.02.009

Lahel, R. S., Kumar, S., & Mishra, R. K. Thanatophoric Dysplasia: Rare Fatal Skeletal Dysplasia Detected on Prenatal Ultrasound (2024). Journal of Medical Ultrasound, 32, 341–344. https://doi.org/10.4103/jmu.jmu_20_23

Li, L., Jin, X., Liu, S., & Fan, H. Prenatal Ultrasound Findings and Prenatal Diagnosis of Fetal Skeletal Dysplasia (2024). Journal of Clinical Ultrasound, 52, 575–587. https://doi.org/10.1002/jcu.23673

Liu, W., Cao, J., Shi, X., et al. Genetic Testing and Diagnostic Strategies of Fetal Skeletal Dysplasia: A Preliminary Study in Wuhan, China (2023). Orphanet Journal of Rare Diseases, 18, 336. https://doi.org/10.1186/s13023-023-02955-4

Nishimura, G., Handa, A., Miyazaki, O., et al. Prenatal Diagnosis of Bone Dysplasias (2023). British Journal of Radiology, 96, 20221025. https://doi.org/10.1259/bjr.20221025

Prawirohardjo, S. Ilmu Kebidanan (Edisi ke-5) (2024). Jakarta: PT Bina Pustaka Sarwono Prawirohardjo.

Royal College of Obstetricians and Gynaecologists. Prenatal Diagnosis and Management of Fetal Abnormalities (2024). London: RCOG Green-top Guideline.

Varney, H., Kriebs, J. M., & Gegor, C. L. Varney’s Midwifery (7th ed.) (2023). Burlington: Jones & Bartlett Learning.

World Health Organization. Birth Defects (2024). Geneva: World Health Organization.

World Health Organization. Standards for Improving Quality of Care for Small and Sick Newborns in Health Facilities (2024). Geneva: World Health Organization.

Xue, H., Yu, A., Zhao, W., et al. Prenatal Diagnosis of Fetal Skeletal Anomalies via Whole-Exome Sequencing in a Tertiary Referral Center (2024). Scientific Reports, 14, 27371. https://doi.org/10.1038/s41598-024-75738-x

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Published

2026-07-20

How to Cite

Nainggolan, Y., Tina, Nasution, E., Zega, A. and Saridatun Nahla, N. (2026) “MIKROMELIA IN NEWBORNS: MIDWIFERY MANAGEMENT AND CLINICAL IMPLICATIONS”, Mitra Husada Health Internasional Conference (MIHHICo), 6(1), pp. 254–259. Available at: https://prosidingmhm.mitrahusada.ac.id/index.php/mihhico/article/view/1969 (Accessed: 30August2026).