Frontiers | Case Report: Blepharophimosis and Ptosis as Leading Dysmorphic Features of Rare Congenital Malformation Syndrome With Developmental Delay – New Cases With TRAF7 Variants
Hypertelorism, wide nasal bridge, bulbous nose with anteverted nares,... | Download Scientific Diagram
Pseudostrabismus - American Academy of Ophthalmology
Mucopolysaccharidosis Type I: Hurler Syndrome - Symptoms & Causes
Mowat-Wilson syndrome: MedlinePlus Genetics
How a family photo could soon diagnose some of the rarest genetic diseases | Daily Mail Online
Population-specific facial traits and diagnosis accuracy of genetic and rare diseases in an admixed Colombian population | Scientific Reports
Prominent nasal bridge and sparse eyebrows. | Download Scientific Diagram
High forehead with flat supraorbital ridges and widely spaced eyes. | Download Scientific Diagram
Apert Syndrome | Children's Hospital of Philadelphia