multiple congenital anomalies/dysmorphic syndrome without intellectual disability hypertrichosis hypertrichosis-acromegaloid facial appearance syndrome https://rarediseases.info.nih.gov/diseases/502/acromegaloid-hypertrichosis-syndrome hypertrichosis-coarse face syndrome SCTID:721837000 acromegaloid facial appearance syndrome and hypertrichosis hypertrichosis-acromegaloid facial features syndrome Hypertrichosis-acromegaloid facial appearance syndrome (HAFF) is a very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis congenita terminalis (thick scalp hair extending onto the forehead with generalized increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows, prominent supraorbital ridges, broad nasal bridge, anteverted nares, long and large philtrum, and prominent mouth with full lips) appearing during childhood. HAFF seems to belong to a spectrum of phenotypes with the clinically overlapping acromegaloid facial appearance syndrome and hypertrichotic osteochondrodysplasia, CantC9 type. Orphanet:966 GARD:0000502 haff acromegaloid hypertrichosis syndrome MONDO:0019940