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wide set eyes flat nasal bridge

How a family photo could soon diagnose some of the rarest genetic diseases  | Daily Mail Online
How a family photo could soon diagnose some of the rarest genetic diseases | Daily Mail Online

Williams syndrome Information | Mount Sinai - New York
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
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

Oculofacial Manifestations of Chromosomal Aberrations | Ento Key
Oculofacial Manifestations of Chromosomal Aberrations | Ento Key

ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson Syndrome -  Ersida Buraniqi, Manikum Moodley, 2015
ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson Syndrome - Ersida Buraniqi, Manikum Moodley, 2015

The face of Smith-Magenis syndrome: a subjective and objective study |  Journal of Medical Genetics
The face of Smith-Magenis syndrome: a subjective and objective study | Journal of Medical Genetics

widely spaced eyes, Hypertelorism as a symptom | FDNA Health
widely spaced eyes, Hypertelorism as a symptom | FDNA Health

Depressed nasal bridge causes: symptom of a rare disease
Depressed nasal bridge causes: symptom of a rare disease

PPT - Jacobsen Syndrome PowerPoint Presentation, free download - ID:1898441
PPT - Jacobsen Syndrome PowerPoint Presentation, free download - ID:1898441

Jacobsen Syndrome: Symptoms, Causes, and Treatments
Jacobsen Syndrome: Symptoms, Causes, and Treatments

Jacobsen syndrome: MedlinePlus Genetics
Jacobsen syndrome: MedlinePlus Genetics

Pseudostrabismus - EyeWiki
Pseudostrabismus - EyeWiki

Frontiers | Case Report: Blepharophimosis and Ptosis as Leading Dysmorphic  Features of Rare Congenital Malformation Syndrome With Developmental Delay  – New Cases With TRAF7 Variants
Frontiers | Case Report: Blepharophimosis and Ptosis as Leading Dysmorphic Features of Rare Congenital Malformation Syndrome With Developmental Delay – New Cases With TRAF7 Variants

Mucopolysaccharidosis Type I: Hurler Syndrome - Symptoms & Causes
Mucopolysaccharidosis Type I: Hurler Syndrome - Symptoms & Causes

Pseudostrabismus - American Association for Pediatric Ophthalmology and  Strabismus
Pseudostrabismus - American Association for Pediatric Ophthalmology and Strabismus

Prominent nasal bridge and sparse eyebrows. | Download Scientific Diagram
Prominent nasal bridge and sparse eyebrows. | Download Scientific Diagram

Mowat-Wilson syndrome: MedlinePlus Genetics
Mowat-Wilson syndrome: MedlinePlus Genetics

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]

Pseudostrabismus - American Academy of Ophthalmology
Pseudostrabismus - American Academy of Ophthalmology

Pseudostrabismus - American Academy of Ophthalmology
Pseudostrabismus - American Academy of Ophthalmology

Hypertelorism - Wikipedia
Hypertelorism - Wikipedia

Apert Syndrome | Children's Hospital of Philadelphia
Apert Syndrome | Children's Hospital of Philadelphia

widely spaced eyes, Hypertelorism as a symptom | FDNA Health
widely spaced eyes, Hypertelorism as a symptom | FDNA Health

Donnai-Barrow syndrome: MedlinePlus Genetics
Donnai-Barrow syndrome: MedlinePlus Genetics

Char syndrome: MedlinePlus Genetics
Char syndrome: MedlinePlus Genetics

Population-specific facial traits and diagnosis accuracy of genetic and  rare diseases in an admixed Colombian population | Scientific Reports
Population-specific facial traits and diagnosis accuracy of genetic and rare diseases in an admixed Colombian population | Scientific Reports