Hypertrichotic osteochondrodysplasia Cantu type
- Synonyms
- Cantu syndrome; Hypertrichotic osteochondrodysplasia
- Modes of inheritance
- Autosomal dominant inheritance (Orphanet)
Not genetically inherited (Orphanet)
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- Chapter Notes
- References
- Authors:
- Dorothy K Grange
- Colin G Nichols
- Gautam K Singh
- view full author information
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (48 available)
Clinical features
Help- Abnormality of head or neck
- Anteverted nares
Anteverted nares
- MedGen UID: 326648
- Concept ID: C1840077
- Finding: Finding
Abnormality of head or neck
- Coarse facial features
Coarse facial features
- MedGen UID: 335284
- Concept ID: C1845847
- Finding: Finding
Abnormality of head or neck
- Depressed nasal bridge
Depressed nasal bridge
- MedGen UID: 373112
- Concept ID: C1836542
- Finding: Finding
Abnormality of head or neck
- Epicanthus
Epicanthus
- MedGen UID: 151862
- Concept ID: C0678230
- Finding: Congenital Abnormality
Abnormality of head or neck
- Gingival overgrowth
Gingival overgrowth
- MedGen UID: 87712
- Concept ID: C0376480
- Finding: Finding
Abnormality of head or neck
- Long philtrum
Long philtrum
- MedGen UID: 351278
- Concept ID: C1865014
- Finding: Finding
Abnormality of head or neck
- Prominent forehead
Prominent forehead
- MedGen UID: 373291
- Concept ID: C1837260
- Finding: Finding
Abnormality of head or neck
- Short neck
Short neck
- MedGen UID: 99267
- Concept ID: C0521525
- Finding: Finding
Abnormality of head or neck
- Thick lower lip vermilion
Thick lower lip vermilion
- MedGen UID: 326567
- Concept ID: C1839739
- Finding: Finding
Abnormality of head or neck
- Thick upper lip vermilion
Thick upper lip vermilion
- MedGen UID: 339521
- Concept ID: C1846423
- Finding: Finding
Abnormality of head or neck
- Wide nasal bridge
Wide nasal bridge
- MedGen UID: 341441
- Concept ID: C1849367
- Finding: Finding
Abnormality of head or neck
- Anteverted nares
- Abnormality of limbs
- Broad first metatarsal
Broad first metatarsal
- MedGen UID: 341001
- Concept ID: C1855899
- Finding: Finding
Abnormality of limbs
- Broad hallux
Broad hallux
- MedGen UID: 401165
- Concept ID: C1867131
- Finding: Finding
Abnormality of limbs
- Coxa valga
Coxa valga
- MedGen UID: 116080
- Concept ID: C0239137
- Finding: Finding
Abnormality of limbs
- Erlenmeyer flask deformity of the femurs
Erlenmeyer flask deformity of the femurs
- MedGen UID: 383796
- Concept ID: C1855895
- Finding: Finding
Abnormality of limbs
- Short hallux
Short hallux
- MedGen UID: 400890
- Concept ID: C1865992
- Finding: Finding
Abnormality of limbs
- Broad first metatarsal
- Abnormality of metabolism/homeostasis
- Lymphedema
Lymphedema
- MedGen UID: 6155
- Concept ID: C0024236
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Lymphedema
- Abnormality of the cardiovascular system
- Bicuspid aortic valve
Bicuspid aortic valve
- MedGen UID: 57436
- Concept ID: C0149630
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Cardiomegaly
Cardiomegaly
- MedGen UID: 5459
- Concept ID: C0018800
- Finding: Finding
Abnormality of the cardiovascular system
- Congenital hypertrophy of left ventricle
Congenital hypertrophy of left ventricle
- MedGen UID: 341003
- Concept ID: C1855901
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Patent ductus arteriosus
Patent ductus arteriosus
- MedGen UID: 4415
- Concept ID: C0013274
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Pericardial effusion
Pericardial effusion
- MedGen UID: 10653
- Concept ID: C0031039
- Finding: Disease or Syndrome
Abnormality of the cardiovascular system
- Bicuspid aortic valve
- Abnormality of the integument
- Congenital, generalized hypertrichosis
Congenital, generalized hypertrichosis
- MedGen UID: 1807304
- Concept ID: C5574955
- Finding: Disease or Syndrome
Abnormality of the integument
- Curly eyelashes
Curly eyelashes
- MedGen UID: 382159
- Concept ID: C2673670
- Finding: Finding
Abnormality of the integument
- Long eyelashes
Long eyelashes
- MedGen UID: 342955
- Concept ID: C1853738
- Finding: Finding
Abnormality of the integument
- Congenital, generalized hypertrichosis
- Abnormality of the musculoskeletal system
- Cuboid-shaped vertebral bodies
Cuboid-shaped vertebral bodies
- MedGen UID: 392973
- Concept ID: C2673653
- Finding: Finding
Abnormality of the musculoskeletal system
- Delayed skeletal maturation
Delayed skeletal maturation
- MedGen UID: 108148
- Concept ID: C0541764
- Finding: Finding
Abnormality of the musculoskeletal system
- Enlarged posterior fossa
Enlarged posterior fossa
- MedGen UID: 340998
- Concept ID: C1855889
- Finding: Finding
Abnormality of the musculoskeletal system
- Hypoplastic ischiopubic ramus
Hypoplastic ischiopubic ramus
- MedGen UID: 870183
- Concept ID: C4024617
- Finding: Finding
Abnormality of the musculoskeletal system
- Large sella turcica
Large sella turcica
- MedGen UID: 334811
- Concept ID: C1843677
- Finding: Finding
Abnormality of the musculoskeletal system
- Macrocephaly
Macrocephaly
- MedGen UID: 745757
- Concept ID: C2243051
- Finding: Finding
Abnormality of the musculoskeletal system
- Metaphyseal widening
Metaphyseal widening
- MedGen UID: 341364
- Concept ID: C1849039
- Finding: Finding
Abnormality of the musculoskeletal system
- Narrow chest
Narrow chest
- MedGen UID: 96528
- Concept ID: C0426790
- Finding: Finding
Abnormality of the musculoskeletal system
- Osteoporosis
Osteoporosis
- MedGen UID: 14535
- Concept ID: C0029456
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Ovoid vertebral bodies
Ovoid vertebral bodies
- MedGen UID: 344549
- Concept ID: C1855665
- Finding: Finding
Abnormality of the musculoskeletal system
- Platyspondyly
Platyspondyly
- MedGen UID: 335010
- Concept ID: C1844704
- Finding: Finding
Abnormality of the musculoskeletal system
- Umbilical hernia
Umbilical hernia
- MedGen UID: 9232
- Concept ID: C0019322
- Finding: Anatomical Abnormality
Abnormality of the musculoskeletal system
- Cuboid-shaped vertebral bodies
- Abnormality of the nervous system
- Intellectual disability, mild
Intellectual disability, mild
- MedGen UID: 10044
- Concept ID: C0026106
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Intellectual disability, mild
- Growth abnormality
- Large for gestational age
Large for gestational age
- MedGen UID: 341215
- Concept ID: C1848395
- Finding: Finding
Growth abnormality
- Large for gestational age
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