Mckusick-kaufman syndrome in an iraqi neonate: a case report

HIGHLIGHTS

  • Who: lenovo from the Department of Pediatrics, College of Medicine, Mustansiriyah University Baghdad, Baghdad, Iraq have published the Article: Pregnancy outcome in a cohort of Egyptian women with rheumatoid arthritis, in the Journal: (JOURNAL) of 10/Oct/2024

SUMMARY

    McKusick-Kaufman syndrome (MKS) is a rare, autosomal recessive disorder, determined by genetic mutation in the MKKS gene on chromosome 20, characterized by a triad of hydrometrocolpos (HMC) in females, post-axial polydactyly, and congenital heart disease, while in males the main documented genital anomalies are hypospadias, cryptorchidism, and chordee. MKS was first described . . .

     

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