Wolf-Hirschhorn Syndrome
Wolf-Hirschhorn Syndrome Wolf-Hirschhorn Syndrome WHS is a rare chromosomal disorder characterized by distinct facial features, d...
Wolf-Hirschhorn Syndrome Wolf-Hirschhorn Syndrome WHS is a rare chromosomal disorder characterized by distinct facial features, d...
Wolf-Hirschhorn Syndrome Wolf-Hirschhorn Syndrome WHS is a rare chromosomal disorder characterized by distinct facial features, d...
Waardenburg Syndrome: A Genetic Journey Through Diversity in Human Pigmentation and Hearing Waardenburg Syndrome (WS) is a rare geneti...
Treacher Collins Syndrome Treacher Collins Syndrome (TCS), also known as mandibulofacial dysostosis, is a complex craniofacial disorder t...
Smith-Lemli-Opitz Syndrome Smith-Lemli-Opitz Syndrome (SLOS) stands as a rare but significant genetic disorder characterized by impair...
Patau Syndrome (Trisomy 13) Patau Syndrome, also known as Trisomy 13, stands as one of the significant chromosomal abnormalities impacting...
**Edward's Syndrome (Trisomy 18): A Profound Portrait of Genetic Complexity** Edward's syndrome, also known as Trisomy 18, represen...
**Cornelia de Lange Syndrome: Navigating the Complexities of a Rare Developmental Disorder** Cornelia de Lange Syndrome (CdLS) stands as a ...