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Flat nasal bridge (also known as depressed nasal bridge) refers to reduced prominence or underdevelopment of the nasal bones and midface, resulting in a flattened appearance of the nose, particularly in profile.
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It can be a normal variant in some populations or a clinical feature of genetic, syndromic, or skeletal disorders, especially those affecting midfacial development.
Anatomical basis
| Structure | Contribution |
|---|---|
| Nasal bones | Provide the bony dorsum of the nose |
| Nasal cartilage | Contributes to tip and alae; not involved in the bridge |
| Midface development | Involves the maxilla and frontal processes; key in syndromic causes |
Flat nasal bridge can be:
A. Genetic Syndromes
| Syndrome | Key Features |
|---|---|
| Down syndrome (Trisomy 21) | Brachycephaly, epicanthal folds, single palmar crease |
| Trisomy 13 (Patau) | Cleft lip/palate, polydactyly, holoprosencephaly |
| Trisomy 18 (Edwards) | Micrognathia, clenched hands, rocker-bottom feet |
| Williams syndrome | Elfin facies, supravalvular aortic stenosis, hypercalcemia |
| ‣ | Hypertelorism, short stature, congenital heart disease |
| Cri-du-chat syndrome | Microcephaly, high-pitched cry, ID |
| ‣ | Smooth philtrum, thin upper lip, short palpebral fissures |
B. Skeletal Dysplasias and Bone Disorders
| Disorder | Features |
|---|---|
| Achondroplasia | Midface hypoplasia, rhizomelic limb shortening |
| Hypochondroplasia | Milder than achondroplasia; flat nasal bridge can occur |
| Thanatophoric dysplasia | Lethal skeletal dysplasia, depressed nasal bridge |
| Cleidocranial dysplasia | Midface hypoplasia, open sutures, absent clavicles |
| Mucopolysaccharidoses (e.g., Hurler syndrome) | Coarse facial features, macrocephaly, corneal clouding |
C. Infectious and Environmental
| Cause | Notes |
|---|---|
| Congenital syphilis | Saddle nose (destruction of nasal cartilage) |
| Fetal alcohol spectrum disorder (FASD) | Includes midface hypoplasia with nasal flattening |
| Congenital Zika syndrome | Microcephaly, midface hypoplasia, calcifications |
A. Fetal Ultrasound (2nd–3rd trimester)
| Measurement | Significance |
|---|---|
| Nasal bone length (NBL) | Short or absent NBL suggests aneuploidy (especially Trisomy 21) |
| Profile view | Helps assess nasal bridge contour and midface hypoplasia |
| Hypoplastic nasal bone | Soft marker for Down syndrome |
B. Postnatal Imaging (X-ray / CT / 3D imaging)