Conradi-Hünermann syndrome

From Wikipedia, the free encyclopedia

Conradi-Hünermann syndrome Classification and external resources
ICD-10	Q 77.3
ICD-9	756.59
OMIM	302960
DiseasesDB	32527

Conradi-Hünermann syndrome is a type of chondrodysplasia punctata.

It is associated with the gene EBP (gene).

[edit] External links

Yahoo health (from NORD)

This disease article is a stub. You can help Wikipedia by expanding it.

v • d • e

Congenital malformations and deformations of musculoskeletal system / musculoskeletal abnormality (Q65-Q79, 754-756)

Congenital limb deformities

Upper limbs	Cleidocranial dysostosis - Madelung's deformity - Sprengel's deformity - Wallis Zieff Goldblatt syndrome

Lower limbs	hip: Dislocation of hip/Hip dysplasia - Upington disease knee: Genu valgum - Genu varum feet: Club foot - Flat feet - Pes cavus

Upper and/or lower limbs	dactyly: Polydactyly/Syndactyly (Webbed toes) - Arachnodactyly - Cenani Lenz syndactylism reduction deficits: Acheiropodia - Amelia - Ectrodactyly - Phocomelia multiple joints: Arthrogryposis - Larsen syndrome

Craniofacial abnormalities

Macrocephaly - Platybasia

Craniosynostosis: Scaphocephaly - Oxycephaly - Trigonocephaly

Craniofacial dysostosis: Crouzon syndrome - Hypertelorism - Hallermann-Streiff syndrome - Treacher Collins syndrome

Craniodiaphyseal dysplasia

Dolichocephaly - Greig cephalopolysyndactyly syndrome - Plagiocephaly

Other axial skeleton

spine: spinal curvature (Scoliosis) - Klippel-Feil syndrome - Spondylolisthesis

ribs: Cervical rib - Bifid rib

sternum: Pectus excavatum - Pectus carinatum

Osteochondrodysplasia

development of cartilage, tubular bones and spine: Achondrogenesis/Hypochondrogenesis - Boomerang dysplasia - Thanatophoric dysplasia - Short rib-polydactyly syndrome - Chondrodysplasia punctata (Rhizomelic chondrodysplasia punctata, Conradi-Hünermann syndrome) - Achondroplasia (Hypochondroplasia) - Osteosclerosis (Raine syndrome) - Ellis-van Creveld syndrome - Otospondylomegaepiphyseal dysplasia - Spondyloepiphyseal dysplasia congenita

collagen diseases: Osteogenesis imperfecta - Ehlers-Danlos syndrome

other: McCune-Albright syndrome - Osteopetrosis - Metaphyseal dysplasia - Recessive multiple epiphyseal dysplasia - Hereditary multiple exostoses - Osteopoikilosis - Chondrodystrophy - Osteodystrophy - Atelosteogenesis, type II - Diastrophic dysplasia - Camurati-Engelmann disease

Other

abdominal wall (Congenital diaphragmatic hernia, Omphalocele, Gastroschisis, Prune belly syndrome)

See also non-congenital conditions (M, 710-739)

Categories: Disease stubs | Skeletal disorders | Congenital disorders

Views

Interaction

Search