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Pear-shaped nose

MedGen UID:
377912
Concept ID:
C1853482
Finding
HPO: HP:0000447

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • Pear-shaped nose

Conditions with this feature

Trichorhinophalangeal dysplasia type I
MedGen UID:
140929
Concept ID:
C0432233
Disease or Syndrome
Trichorhinophalangeal syndrome (TRPS) comprises TRPS I (caused by a heterozygous pathogenic variant in TRPS1) and TRPS II (caused by contiguous gene deletion of TRPS1, RAD21, and EXT1). Both types of TRPS are characterized by distinctive facial features; ectodermal features (fine, sparse, depigmented, and slow growing hair; dystrophic nails; and small breasts); and skeletal findings (short stature; short feet; brachydactyly with ulnar or radial deviation of the fingers; and early, marked hip dysplasia). TRPS II is characterized by multiple osteochondromas (typically first observed clinically on the scapulae and around the elbows and knees between ages 1 month and 6 years) and an increased risk of mild-to-moderate intellectual disability.
Intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism
MedGen UID:
342889
Concept ID:
C1853480
Disease or Syndrome
Trichorhinophalangeal syndrome, type III
MedGen UID:
349899
Concept ID:
C1860823
Disease or Syndrome
Trichorhinophalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Craniofacial features include sparse, slowly growing scalp hair, laterally sparse eyebrows, a bulbous tip of the nose, protruding ears, long flat philtrum, and thin upper vermillion border. The most typical radiographic findings in TRPS are cone-shaped epiphyses, predominantly at the middle phalanges. Hip malformations such as coxa plana, coxa magna, or coxa vara are present in over 70% of patients. In older patients, the hip abnormalities resemble degenerative arthrosis. TRPS3 differs from TRPS1 by the presence of severe brachydactyly, due to short metacarpals, and severe short stature (summary by Ludecke et al., 2001).
Koolen-de Vries syndrome
MedGen UID:
355853
Concept ID:
C1864871
Disease or Syndrome
Koolen-de Vries syndrome (KdVS) is characterized by developmental delay / intellectual disability, neonatal/childhood hypotonia, dysmorphisms, congenital malformations, and behavioral features. Psychomotor developmental delay is noted in all individuals from an early age. The majority of individuals with KdVS function in the mild-to-moderate range of intellectual disability. Other findings include speech and language delay (100%), epilepsy (~33%), congenital heart defects (25%-50%), renal and urologic anomalies (25%-50%), and cryptorchidism (71% of males). Behavior in most is described as friendly, amiable, and cooperative.

Professional guidelines

PubMed

Yan Y, Huang S, Huang L, Zhang J, Li S, Zhang C, Luo X
Horm Res Paediatr 2024;97(1):28-39. Epub 2023 Mar 29 doi: 10.1159/000530414. PMID: 36990068

Recent clinical studies

Etiology

Ning CC, Hsu MM, Lee JY, Chao SC
J Formos Med Assoc 2001 Sep;100(9):635-8. PMID: 11695282

Diagnosis

Smaili W, Elalaoui SC, Meier S, Zerkaoui M, Sefiani A, Heinimann K
BMC Med Genet 2017 May 3;18(1):50. doi: 10.1186/s12881-017-0413-8. PMID: 28468609Free PMC Article
Pereda A, Azriel S, Bonet M, Garin I, Gener B, Lecumberri B, de Nanclares GP
J Pediatr Endocrinol Metab 2014 Nov;27(11-12):1089-94. doi: 10.1515/jpem-2014-0020. PMID: 24945424
Bottero L, Cinalli G, Labrune P, Lajeunie E, Renier D
Childs Nerv Syst 1997 May;13(5):275-80; discussion 281. doi: 10.1007/s003810050082. PMID: 9224917
Itin PH, Bohn S, Mathys D, Guggenheim R, Richard G
Dermatology 1996;193(4):349-52. doi: 10.1159/000246290. PMID: 8993967
Carrington PR, Chen H, Altick JA
J Am Acad Dermatol 1994 Aug;31(2 Pt 2):331-6. doi: 10.1016/s0190-9622(94)70166-0. PMID: 8034799

Prognosis

Bottero L, Cinalli G, Labrune P, Lajeunie E, Renier D
Childs Nerv Syst 1997 May;13(5):275-80; discussion 281. doi: 10.1007/s003810050082. PMID: 9224917

Clinical prediction guides

Su W, Shi X, Lin M, Huang C, Wang L, Song H, Zhuang Y, Zhang H, Li N, Li X
BMC Med Genet 2018 Dec 12;19(1):211. doi: 10.1186/s12881-018-0732-4. PMID: 30541476Free PMC Article
Smaili W, Elalaoui SC, Meier S, Zerkaoui M, Sefiani A, Heinimann K
BMC Med Genet 2017 May 3;18(1):50. doi: 10.1186/s12881-017-0413-8. PMID: 28468609Free PMC Article
Seitz CS, Lüdecke HJ, Wagner N, Bröcker EB, Hamm H
Arch Dermatol 2001 Nov;137(11):1437-42. doi: 10.1001/archderm.137.11.1437. PMID: 11708946
Vilain C, Sznajer Y, Rypens F, Désir D, Abramowicz MJ
Am J Med Genet 1999 Aug 27;85(5):495-7. PMID: 10405449
McCloud DJ, Solomon LM
Br J Dermatol 1977 Apr;96(4):403-7. doi: 10.1111/j.1365-2133.1977.tb07136.x. PMID: 861178

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