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fence set a fire lobby wide set eyes flat nasal bridge Make a bed fall back Perch

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

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

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

Facial Phenotypes – Kleefstra syndrome
Facial Phenotypes – Kleefstra syndrome

Apert Syndrome: Practice Essentials, Pathophysiology, Epidemiology
Apert Syndrome: Practice Essentials, Pathophysiology, Epidemiology

Genetic Syndromes - Don't Forget the Bubbles
Genetic Syndromes - Don't Forget the Bubbles

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

High forehead with flat supraorbital ridges and widely spaced eyes. |  Download Scientific Diagram
High forehead with flat supraorbital ridges and widely spaced eyes. | Download Scientific Diagram

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]

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

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

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

Jacobsen syndrome: MedlinePlus Genetics
Jacobsen syndrome: MedlinePlus Genetics

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

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

CDK13-related disorder - Wikipedia
CDK13-related disorder - Wikipedia

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

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

Kaufman oculocerebrofacial syndrome: MedlinePlus Genetics
Kaufman oculocerebrofacial syndrome: MedlinePlus Genetics

Hypertelorism, wide nasal bridge, bulbous nose with anteverted nares,... |  Download Scientific Diagram
Hypertelorism, wide nasal bridge, bulbous nose with anteverted nares,... | Download Scientific Diagram

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

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

Char syndrome: MedlinePlus Genetics
Char syndrome: MedlinePlus Genetics

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