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Treacher Collins Syndrome
Treacher Collins syndrome
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Related in the Kosmos
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Oral and maxillofacial surgery
Craniofacial
Crouzon syndrome
Craniosynostosis
Cleft palate
Micrognathia
Syndromes
(18)
Wallis Zieff Goldblatt syndrome
Rapadilino syndrome
Apert syndrome
Hallermann Streiff syndrome
Greig cephalopol- ysyndactyly syndrome
Greig cephalopol- ysyndactyly syndrome
Larsen syndrome
Waardenburg syndrome
Fetofetal transfusion
Trisomy 13
Turner syndrome
Hereditary sensory and autonomic neuropathies
Trisomy 18
Pierre Robin Sequence
Noonan syndrome
Triplo X syndrome
Alport syndrome
Thymic aplasia
Crouzon syndrome
more...
Genodermatoses
Mandibulofacial dysostosis
Apert syndrome
Crouzon syndrome
Turner syndrome
Noonan syndrome
Rare diseases
(12)
Upington disease
Acheiropodia
Cenani Lenz syndactylism
Arthrogryposis
Nager syndrome
Nager syndrome
Leukodystrophy, globoid cell
Triose Phosphate Isomerase deficiency
Thanatophoric dysplasia
Wallis Zieff Goldblatt syndrome
Rapadilino syndrome
Hallermann Streiff syndrome
Larsen syndrome
more...
Genetic disorders
(32)
Arachnodactyly
Thrombocytopenia absent radius
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Glutaricaciduria
Glutaricaciduria
Spondyloepiphyseal dysplasia congenita
Langer-giedion syndrome
VATER syndrome
Galactosemias
Shwachman syndrome
Upington disease
Wallis Zieff Goldblatt syndrome
Acheiropodia
Cenani Lenz syndactylism
Rapadilino syndrome
Apert syndrome
Hallermann Streiff syndrome
Greig cephalopol- ysyndactyly syndrome
Larsen syndrome
Waardenburg syndrome
Trisomy 13
Crouzon syndrome
Turner syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Trisomy 18
Noonan syndrome
Triose Phosphate Isomerase deficiency
Triplo X syndrome
Alport syndrome
Thanatophoric dysplasia
Thymic aplasia
more...
Congenital disorders
(13)
Amelia (birth defect)
Dysmelia
Abdominal wall defect
Congenital malformations
Oxycephaly
Oxycephaly
Goldenhar
Craniofacial microsomia
Acheiropodia
Cenani Lenz syndactylism
Arthrogryposis
Genetic disorders
Nager syndrome
Cleft palate
more...
Diseases and disorders
(16)
Platybasia
Coxa valga
Metaphyseal dysplasia
Atresia
Short rib-polydactyly syndrome
Short rib-polydactyly syndrome
Lupus erythematosus, cutaneous
Dislocation of hip
Amelia (birth defect)
Upington disease
Wallis Zieff Goldblatt syndrome
Rapadilino syndrome
Hallermann Streiff syndrome
Oxycephaly
Leukodystrophy, globoid cell
Micrognathia
VATER syndrome
more...
Congenital heart disease
Transposition of great vessels
Tricuspid atresia
Persistent truncus arteriosus
Pediatrics
(8)
Neonatal hyperbilirubinemia
Purpura, schoenlein-henoch
Larsen syndrome
Hyperostosis, cortical, congenital
Tricuspid atresia
Tricuspid atresia
Craniosynostosis
Persistent truncus arteriosus
Shwachman syndrome
more...
Medical condition
(70)
Microtia
Turner-like syndrome
Trichiniasis
Sarcomas
Tuberculosis
Tuberculosis
Coloboma
Mohr syndrome
Myopathies, structural, congenital
Glossopharyngeal nerve diseases
Conductive hearing loss
Type i complex regional pain syndrome
Craniofrontonasal dysplasia
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Tracheoesophageal fistula
Nager & miller
Thoracic celosomia
Tyrosine-oxidase temporary deficiency
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Floating harbor syndrome
Intervertebral disk displacement
Rosenthal syndrome
Mandibulofacial dysostosis
Upington disease
Acheiropodia
Rapadilino syndrome
Arthrogryposis
Hyperlipop- roteinemia type I
Apert syndrome
Transposition of great vessels
Greig cephalopol- ysyndactyly syndrome
Arachnodactyly
Neonatal hyperbilirubinemia
Larsen syndrome
Thrombocytopenia absent radius
Waardenburg syndrome
Hyperostosis, cortical, congenital
Fetofetal transfusion
Tricuspid atresia
Trisomy 13
Crouzon syndrome
Craniosynostosis
Persistent truncus arteriosus
Purpura, schoenlein-henoch
Short rib-polydactyly syndrome
Cleft palate
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Craniofacial microsomia
Trisomy 18
Glutaricaciduria
Pierre Robin Sequence
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Noonan syndrome
Triose Phosphate Isomerase deficiency
Triplo X syndrome
Dislocation of hip
Spondyloepiphyseal dysplasia congenita
Langer-giedion syndrome
Alport syndrome
Thanatophoric dysplasia
VATER syndrome
Galactosemias
Shwachman syndrome
Thymic aplasia
Brachial plexus neuropathies
more...
See also
(20)
Treacher Collins-Fr- anceschetti syndrome 1
Edward Treacher Collins
Bifid rib
Hyperlipop- roteinemia type I
Musculoskeletal system
Musculoskeletal system
Transtentorial herniation
Tongue inflammation
Polyendocr- inopathies, autoimmune
Axial skeleton
Connective tissue
Autosomal dominant
Genetic counseling
Hearing impairment
Hearing loss with craniofacial syndromes
Low-set ears
Receding chin
Trigonocephaly
Vision problems
Www.treach- ercollinsfnd.org
Julianna Wetmore
more...
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