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Achondrogenesis Syndrome


Achondrogenesis affects approximately 1 out of every 50,000 births. Bone and cartilage development is affected by this severe genetic disorder.

A child that is born with achondrogenesis will usually have a small body with short arms and legs. They may also suffer with a small chest, enlarged abdomen and breathing difficulties from immature lungs.

Children with this condition may have a distinct forehead, small chin and cleft palate. Although some children have survived for a short amount of time with medical care, it is common for most infants to die from the condition. It can cause premature birth or stillbirth.





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  • 1A1V-(Single-Umbilical-Artery) 12
  • Achondrogenesis-Syndrome 0
  • Achondroplasia 0
  • Allan-Herndon-Dudley-Syndrome 0
  • Alstrom-Syndrome 0
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  • Beckwith-Wiedemann-Syndrome 1
  • Bloom-Syndrome 0
  • Branchial-Cleft-Cyst 0
  • Calcaneovalgus 0
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  • Cat-Eye-Syndrome 5
  • Cerebral-Palsy 3
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  • CHARGE-Syndrome 0
  • Choroid-Plexus-Cysts-(CPC) 10
  • Cleft-Lip,-Cleft-Palate 13
  • Cleidocranial-Dysplasia 1
  • Clubfoot 12
  • Cockayne-Syndrome 0
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  • Congenital-Heart-Defect 12
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  • Fetal-Alcohol-Syndrome 1
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  • Fryns-Syndrome 0
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  • Gastroschisis 5
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  • Hemangioma 5
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  • Hip-Dysplasia 1
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  • Holt-Oram-Syndrome 0
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  • Hypospadias 8
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  • Iniencephaly 0
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  • Jackson-Weiss-Syndrome 0
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  • Jeune-Syndrome 0
  • Joubert-Syndrome 1
  • Juberg-Marsidi-Syndrome 0
  • Kasabach-Merritt-Syndrome 0
  • Klippel-Feil-Syndrome 0
  • Klippel-Trenaunay-Syndrome 0
  • L1-Syndrome 0
  • Labial-Fusion 0
  • Laurence-Moon-Syndrome 0
  • LEOPARD-Syndrome 0
  • Leri-Weil-Syndrome 1
  • Lissencephaly 0
  • Lowe-Syndrome 0
  • Marfan-Syndrome 0
  • McCune-Albright-Syndrome 0
  • McKusick-Kaufman-Syndrome 0
  • Meckel-Gruber-Syndrome 0
  • Meckel`s-Diverticulum 0
  • Megalencephaly 0
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  • Miller-Syndrome 0
  • Moebius-Syndrome 0
  • Muenke-Syndrome 0
  • Multicystic-Dysplastic-Kidneys 0
  • Myelomeningocele 0
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  • Nail-Patella-Syndrome 0
  • Neuronal-Migration-Disorder 0
  • Noonan-Syndrome 0
  • Norrie-Disease 0
  • Ollier`s-Disease 1
  • Omphalocele 1
  • Opitz-G-BBB-Syndrome 0
  • Osteogenesis-Imperfecta 0
  • Parry-Romberg-Syndrome 0
  • Pectus-Carinatum 0
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  • Penile-Agenesis 0
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  • Phenylketonuria-(PKU) 0
  • Pierre-Robin-Sequence 0
  • Platyspondylic-Lethal-Skeletal-Dysplasia 0
  • Poland-Syndrome 0
  • Polydactyly 0
  • Polymicrogyria 0
  • Porencephaly 0
  • Port-Wine-Stain 0
  • Posterior-Urethral-Valves 1
  • Prader-Willi-Syndrome 0
  • Progeria 0
  • Prune-Belly-Syndrome 0
  • Renal-Agenesis 4
  • Rett-Syndrome 1
  • Roberts-Syndrome 0
  • Robinow-Syndrome 0
  • Rothmund-Thomson-Syndrome 0
  • Rubinstein-Taybi-Syndrome 0
  • Russell-Silver-Syndrome 0
  • Schizencephaly 0
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  • Smith-Magenis-Syndrome 0
  • Soto`s-Syndrome 0
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  • Stork-Bites 9
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  • Syndactyly 0
  • Tay-Sachs-Disease 0
  • test 2
  • Tethered-Spinal-Cord-Syndrome 1
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  • Tetrasomy-X-Syndrome 0
  • Thalassaemia-Major 0
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  • Trisomy-18 3
  • Trisomy-21 7 (1 new)
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  • Umbilical-Hernia 7
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  • Vaginal-Agenesis 0
  • Velocardiofacial-Syndrome 0
  • Ventricular-Septal-Defect 2
  • Waardenburg-Syndrome 0
  • Wolf-Hirschhorn-Syndrome 1

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