Pseudostrabismus - American Academy of Ophthalmology
Frontiers | Case Report: Blepharophimosis and Ptosis as Leading Dysmorphic Features of Rare Congenital Malformation Syndrome With Developmental Delay – New Cases With TRAF7 Variants
ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson Syndrome - Ersida Buraniqi, Manikum Moodley, 2015
Williams syndrome Information | Mount Sinai - New York
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
Facial Phenotypes – Kleefstra syndrome
Depressed nasal bridge causes: symptom of a rare disease
![Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2021;26:31-33]](https://www.hkjpaed.org/figure/2021;26;31-33-fig1.jpg "Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2021;26:31-33]")
Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2021;26:31-33]
Hypertelorism - Wikipedia
Worried about my baby | BabyCenter
Pseudostrabismus - American Association for Pediatric Ophthalmology and Strabismus
Donnai-Barrow syndrome: MedlinePlus Genetics
Fetal Alcohol Syndrome - Guyana Chronicle
CDK13-related disorder - Wikipedia
Oculofacial Manifestations of Chromosomal Aberrations | Ento Key
widely spaced eyes, Hypertelorism as a symptom | FDNA Health
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
High forehead with flat supraorbital ridges and widely spaced eyes. | Download Scientific Diagram
Down Syndrome - Pathology Flashcards | ditki medical and biological sciences
Char syndrome: MedlinePlus Genetics
Apert Syndrome | Children's Hospital of Philadelphia
Mowat-Wilson syndrome: MedlinePlus Genetics
PPT - Jacobsen Syndrome PowerPoint Presentation, free download - ID:1898441
