Coexistence of molybdenum cofactor deficiency type A and hypertrophic pyloric stenosis, a new case

SATAR M., KURTOĞLU A. İ., YAPICIOĞLU YILDIZDAŞ H., ÖNENLİ MUNGAN H. N., ÖZLÜ F., BİŞGİN A.

TURKISH ARCHIVES OF PEDIATRICS, cilt.56, sa.1, ss.78-80, 2021 (ESCI) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 56 Sayı: 1
  • Basım Tarihi: 2021
  • Doi Numarası: 10.14744/turkpediatriars.2020.57984
  • Dergi Adı: TURKISH ARCHIVES OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.78-80
  • Anahtar Kelimeler: Molybdenum cofactor deficiency type A, newborn, pyloric stenosis
  • Çukurova Üniversitesi Adresli: Evet

Özet

Molybdenum cofactor deficiency is a rare neurometabolic disease that is usually characterized by seizures, abnormal muscle tonus, developmental delay and poor nutrition, and is seen soon after birth. Pyloric stenosis causes serious vomiting in the first months of life. The presence of neurologic damage in molybdenum cofactor deficiency and possible abnormal innervations may cause pyloric stenosis; however, the pathogenesis is unclear. Pyloric stenosis with molybdenum cofactor deficiency has been described in two cases. Herein, we report the third case and suggest that hypertrophic pyloric stenosis should be kept in mind as a clinical manifestation of molybdenum cofactor deficiency.