Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Epidemiological and Clinical Profile of Cleft Lip and/or Palate in Mbujimayi: A Cross-Sectional Study.

Created on 03 Sep 2026

Authors

Trésor Kabuya Kabamba, Eugène Mukeba Bamusua, Pascal Cimpaka Kabeya, Pascal Kayembe Shambuyi, Micheline Nyembo Epupwa, Didier Mubenga Katende, Séraphin Binene Katulondi, Henry-Benjamin Tshimanga Kabeya, Jenny Nshimba Kabemba, Joël Manyonga, Joseph Luboya Kabila, Hubert Kabanga Ngandu, Roger Kamwema Shamuana, François Kabumba Kabumba

Published in

Health science reports. Volume 9. Issue 9. Pages e73171. Epub Sep 01, 2026.

Abstract

Cleft lip and/or palate (CLP) is the most common craniofacial malformation worldwide, with significant geographic and socioeconomic disparities. In Mbujimayi, DRC, no prior data have been published on its prevalence or clinical presentation. This study aimed to determine the epidemiological and clinical profile of CLP in Mbujimayi.
This was a cross‑sectional study conducted at the University Clinics of Mbujimayi between March 2023 and July 2025. A total of 54 patients with CLP were included. Ethical approval was obtained. Data were collected on demographic characteristics, anatomical types of CLP, and associated complications.
Unilateral cleft lip was the most frequent anatomical type, predominantly affecting the left side (48.1%). The mean age of patients was 5.5 years, with extremes ranging from 0.5 to 20 years. Feeding difficulties (40.7%), speech disorders, malnutrition, and social integration challenges (27.8%) were among the most common complications. A family history of CLP was reported in 13.0% of cases, and one associated malformation (cryptorchidism) was noted. The absence of a regional registry and reliance on free surgical campaigns limited the assessment of prevalence and postoperative outcomes.
CLP is relatively common in Mbujimayi and is accompanied by significant clinical and psychosocial complications. Its management remains a major challenge in this resource-limited setting. The establishment of a congenital malformation registry and structured follow-up programs is essential to improve care and guide future research.
Not applicable.

PMID:
42688352
Bibliographic data and abstract were imported from PubMed on 03 Sep 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 9
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement