How a family photo could soon diagnose some of the rarest genetic diseases | Daily Mail Online
Pseudostrabismus - American Academy of Ophthalmology
Pseudostrabismus - EyeWiki
ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson Syndrome - Ersida Buraniqi, Manikum Moodley, 2015
Apert Syndrome: Practice Essentials, Pathophysiology, Epidemiology
Apert Syndrome | Children's Hospital of Philadelphia
widely spaced eyes, Hypertelorism as a symptom | FDNA Health
Oculofacial Manifestations of Chromosomal Aberrations | Ento Key
Facial Phenotypes – Kleefstra syndrome
Jacobsen syndrome: MedlinePlus Genetics
The face of Smith-Magenis syndrome: a subjective and objective study | Journal of Medical Genetics
Down Syndrome - Pathology Flashcards | ditki medical and biological sciences
Mucopolysaccharidosis Type I: Hurler Syndrome - Symptoms & Causes
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
widely spaced eyes, Hypertelorism as a symptom | FDNA Health
Momimus on X: "@davenewworld_2 The wide set eyes, epicanthal folds, and low nasal bridge look very indicative of FAS, that would explain why her face is odd - and it could also