Rare diseases · Sign or symptom
Thickened nuchal skin fold
Thickened skin folds of neck
HP:0000474
What it means
A thickening of the skin thickness in the posterior aspect of the fetal neck. A nuchal fold (NF) measurement is obtained in a transverse section of the fetal head at the level of the cavum septum pellucidum and thalami, angled posteriorly to include the cerebellum. The measurement is taken from the outer edge of the occiput bone to the outer skin limit directly in the midline. An NF measurement greater than 5 mm at 14 to 17+6 weeks of gestation, or 6 mm at 18 to 28 weeks has been associated with a markedly increased risk for Down syndrome.
The measurement of nuchal fold (NF) thickness during the second trimester is considered to be one of the most sensitive and specific isolated ultrasound marker for the identification of suspected cases of trisomy 21. Thick NF may also be seen in other aneuploidies as well as Turner's syndrome, Noonan's syndrome, Roberts syndrome, Zellweger syndrome and with congenital heart disease and with pathogenic CNVs. A thickened nuchal fold should be distinguished from cystic hygroma, in which the skin in this area has fluid-filled loculations. A thickened nuchal fold should not be confused with nuchal translucency, which is a specific measurement of fluid in the posterior aspect of the neck at 11 to 14 weeks gestation (see practice guidelines at http://www.sogc.org).
Rare diseases that can present with this31
Very common80–99%
12- Achondrogenesis
- Achondrogenesis type 1A
- Achondrogenesis type 1B
- Behavioral variant of frontotemporal dementia
- Distal duplication 18q syndrome
- Down syndrome
- Dysmorphism-cleft palate-loose skin syndrome
- Noonan syndrome
- Postaxial polydactyly-dental and vertebral anomalies syndrome
- Progressive non-fluent aphasia
- Pseudoxanthoma elasticum
- Trisomy 12p syndrome
Common30–79%
15- Costello syndrome
- Craniofrontonasal dysplasia
- DOORS syndrome
- Fetal hydantoin syndrome
- Fryns syndrome
- MEND syndrome
- Microcephalic osteodysplastic primordial dwarfism types I and III
- Monosomy X syndrome
- Mosaic monosomy X syndrome
- Phosphoserine aminotransferase deficiency, infantile/juvenile form
- Prominent glabella-microcephaly-hypogenitalism syndrome
- Tetrasomy 21 syndrome
- Turner syndrome
- Turner syndrome due to structural X chromosome anomalies
- Velo-facial-skeletal syndrome
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Excess nuchal skin · Increased nuchal fold · Increased nuchal fold thickness · Thick nuchal fold · Thickened nuchal skin · Thickened skin over the neck
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Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.