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SpecialtyMedical genetics


Achondrogenesis is a group of severe disorders that affect cartilage and bone development. These conditions are characterized by a small body, short limbs, and other skeletal abnormalities.

Achondrogenesis type I.jpg
Achondrogenesis type I radiogram.jpg
Achondrogenesis type I usg.jpg


  • Researchers have described at least three forms of achondrogenesis, designated as type 1A, type 1B, and type 2.
  • The types are distinguished by their signs and symptoms, inheritance pattern, and genetic cause. However, types 1A and 1B are often hard to tell apart without genetic testing.


Achondrogenesis types 1A and 1B are rare genetic disorders; their incidence is unknown. Combined, achondrogenesis type 2 and hypochondrogenesis (a similar skeletal disorder) occur in 1 in 40,000 to 60,000 newborns.


Mutations in the TRIP11, SLC26A2, and COL2A1 genes cause achondrogenesis type 1A, type 1B, and type 2, respectively. TYype 1A

  • The genetic cause of achondrogenesis type 1A was unknown until recently, when researchers discovered that the condition can result from mutations in the TRIP11 gene.
  • This gene provides instructions for making a protein called GMAP-210.
  • This protein plays a critical role in the Golgi apparatus, a cell structure in which newly produced proteins are modified so they can carry out their functions.
  • Mutations in the TRIP11 gene prevent the production of functional GMAP-210, which alters the structure and function of the Golgi apparatus.
  • Researchers suspect that cells called chondrocytes in the developing skeleton may be most sensitive to these changes. Chondrocytes give rise to cartilage, a tough, flexible tissue that makes up much of the skeleton during early development.
  • Most cartilage is later converted to bone, except for the cartilage that continues to cover and protect the ends of bones and is present in the nose and external ears.
  • Malfunction of the Golgi apparatus in chondrocytes likely underlies the problems with bone formation in achondrogenesis type 1A.

Type 1B Achondrogenesis type 1B is the most severe of a spectrum of skeletal disorders caused by mutations in the SLC26A2 gene. This gene provides instructions for making a protein that is essential for the normal development of cartilage and for its conversion to bone. Mutations in the SLC26A2 gene cause the skeletal problems characteristic of achondrogenesis type 1B by disrupting the structure of developing cartilage, which prevents bones from forming properly.

Type 2

  • Achondrogenesis type 2 is one of several skeletal disorders that result from mutations in the COL2A1 gene.
  • This gene provides instructions for making a protein that forms type II collagen.
  • This type of collagen is found mostly in cartilage and in the clear gel that fills the eyeball (the vitreous).
  • It is essential for the normal development of bones and other connective tissues that form the body's supportive framework.
  • Mutations in the COL2A1 gene interfere with the assembly of type II collagen molecules, which prevents bones and other connective tissues from developing properly.


Autosomal recessive inheritance, a 25% chance
  • Achondrogenesis type 1A and type 1B both have an autosomal recessive pattern of inheritance, which means both copies of the TRIP11 or SLC26A2 gene in each cell have mutations. Most often, the parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene but do not show signs and symptoms of the condition.
Autosomal dominant pattern, a 50/50 chance.
  • Achondrogenesis type 2 is considered an autosomal dominant disorder because one copy of the altered gene in each cell is sufficient to cause the condition. It is almost always caused by new mutations in the COL2A1 gene and typically occurs in people with no history of the disorder in their family.

Signs and symptoms

Type 1A Achondrogenesis type 1A, which is also called the Houston-Harris type, is the least well understood of the three forms. Affected infants have extremely short limbs, a narrow chest, short ribs that fracture easily, and a lack of normal bone formation (ossification) in the skull, spine, and pelvis.

Type 1B Achondrogenesis type 1B, also known as the Parenti-Fraccaro type, is characterized by extremely short limbs, a narrow chest, and a prominent, rounded abdomen. The fingers and toes are short and the feet may turn inward and upward (clubfeet). Affected infants frequently have a soft out-pouching around the belly-button (an umbilical hernia) or near the groin (an inguinal hernia).[1][1].

Type 2 Infants with achondrogenesis type 2, which is sometimes called the Langer-Saldino type, have short arms and legs, a narrow chest with short ribs, and underdeveloped lungs. This condition is also associated with a lack of ossification in the spine and pelvis. Distinctive facial features include a prominent forehead, a small chin, and, in some cases, an opening in the roof of the mouth (a cleft palate). The abdomen is enlarged, and affected infants often have a condition called hydrops fetalis, in which excess fluid builds up in the body before birth.

For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. 80%-99% of people have these symptoms

  • Abnormal enchondral ossification
  • Abnormality of bone mineral density
  • Anteverted nares(Nasal tip, upturned)
  • Aplasia/Hypoplasia of the lungs(Absent/small lungs)
  • Flat face(Flat facial shape)
  • Frontal bossing
  • Long philtrum
  • Macrocephaly(Increased size of skull)
  • Micrognathia(Little lower jaw)
  • Narrow chest(Low chest circumference)
  • Severe short stature(Dwarfism)
  • Short neck(Decreased length of neck)
  • Short nose(Decreased length of nose)
  • Short thorax(Shorter than typical length between neck and abdomen)
  • Skeletal dysplasia
  • Thickened nuchal skin fold(Thickened skin folds of neck)

30%-79% of people have these symptoms

5%-29% of people have these symptoms

  • Abnormality of cardiovascular system morphology
  • Cystic hygroma


  • Achondrogenesis can be diagnosed during pregnancy by ultrasound as early as 12-14 weeks. At birth, this condition is suspected when the infant has extremely short underdeveloped arms and legs, short ribs and small chest, and short trunk.
  • X-ray findings include underdeveloped skull, vertebrate and rib cage.
  • Genetic testing of the TRIP11, SLC26A2 and COL2A1 genes can be performed to confirm the diagnosis and determine the type of achondrogenesis.


  • Medical care for achondrogenesis is focused on addressing any symptoms and relieving pain.
  • Genetic counseling is recommended for families with a diagnosis of achondrogenesis.


Most infants with achondrogenesis have severely underdeveloped lungs which leads to serious breathing problems and lung failure. Most die before or shortly after birth because of the severity of this disorder.


  1. Bonafé L, Mittaz-Crettol L, Ballhausen D, et al. Achondrogenesis Type 1B. 2002 Aug 30 [Updated 2013 Nov 14]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020. Available from:


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