# Bartsocas-Papas syndrome: The first case report of severe autosomal recessive form from Indonesia
> Josh F.

URL kanonis: https://discover.unhas.ac.id/publications/pub_scopus_85100124242
Jurnal / Konferensi: International Journal of Surgery Case Reports
Tahun terbit: 2021
DOI: https://doi.org/10.1016/j.ijscr.2021.01.070
ISSN: 22102612
Kuartil SJR: Q3
Citations: 3

## Authors
- Josh F.

## Abstract
INTRODUCTION: Bartsocas-Papas syndrome (BPS) is an autosomal recessive form of Popliteal Pterygium syndrome (PPS). It is a very rare disease characterized by congenital craniofacial anomalies, popliteal webbing, and genitourinary and musculoskeletal anomalies. Almost all of the cases were reported in dead intrauterine pregnancies. PRESENTATION OF CASE: We present a 10-month-old boy with bilateral complete cleft lip and palate, abnormal scalp hair, an absence of both upper eyelids, choanal atresia, syndactyly of the third and fourth fingers of the right hand, agenesis fingers on the left hand, bilateral popliteal pterygia, bilateral talipes equinovarus, agenesis of the toes of both lower extremities, intercrural webbing, an absence of testis, and scrotal anomaly. Multistage surgical correction was performed for the multiple congenital malformations. CONCLUSION: We report the first case of BPS from Indonesia. Gradual management should be performed according to the patient's age and available facilities.

## Keywords
- Medicine
- Craniofacial
- Genitourinary system
- Dermatology
- Pediatrics
- Anatomy
- Psychiatry

---
Sumber: Discover Unhas — RIMS Universitas Hasanuddin.
Saat mengutip, gunakan DOI bila tersedia atau URL kanonis di atas.