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Cerebro facio thoracic dysplasia(CFSMR)

MedGen UID:
347111
Concept ID:
C1859252
Disease or Syndrome
Synonym: Cerebrofaciothoracic Dysplasia
SNOMED CT: Cerebro-facio-thoracic dysplasia (720635002); Pascual Castroviejo syndrome type 1 (720635002)
 
OMIM®: 213980

Definition

Cerebro-facio-thoracic dysplasia is a rare condition characterized by abnormal development (dysplasia) of the brain (cerebro) and structures in the face (facio) and torso (thoracic). The problems with development lead to the key features of cerebro-facio-thoracic dysplasia, which include severe intellectual disability, distinctive facial features, and abnormalities of the ribs and spinal bones (vertebrae).

In addition to intellectual disability, individuals with cerebro-facio-thoracic dysplasia have delayed development of speech and movement (motor) skills, and in some, these skills never develop. Nearly one-quarter of affected individuals never learn to speak and almost half are unable to walk. Weak muscle tone (hypotonia) and difficulty feeding occur in some affected infants. People with cerebro-facio-thoracic dysplasia can have neurodevelopmental problems, such as anxiety, autism spectrum disorder, or self-injuring behavior; however, many people with the condition are described as friendly and good-natured.

Distinctive facial features common in cerebro-facio-thoracic dysplasia include a wide, short skull (brachycephaly); highly arched eyebrows or eyebrows that grow together in the middle (synophrys); widely spaced eyes (hypertelorism); a wide nasal bridge; low-set ears; an upper lip with pronounced curves (Cupid's bow upper lip); and small teeth (microdontia). Some affected individuals have overgrowth of the gums (gingival hyperplasia), an opening in the roof of the mouth (cleft palate), or a split in the upper lip (cleft lip).

Problems with bone development in the torso (thorax) commonly leads to bone abnormalities such as two or more ribs that are joined together (fused) or ribs that are abnormally shaped with two prongs at one end (bifid ribs). Many people with cerebro-facio-thoracic dysplasia have abnormal side-to-side curvature of the spine (scoliosis) due to malformation of the vertebrae; some vertebrae may also be fused. Additionally, the shoulder blades can be affected in people with this condition.

A wide variety of other features can occur in cerebro-facio-thoracic dysplasia, such as abnormalities involving the eyes, skin, or hair. Heart defects, digestive problems, or genitourinary problems (such as abnormal kidneys or reproductive organs) can also occur. Affected individuals may also have bone or joint abnormalities in other parts of the body. [from MedlinePlus Genetics]

Recent clinical studies

Diagnosis

Sharkia R, Zalan A, Jabareen-Masri A, Hengel H, Schöls L, Kessel A, Azem A, Mahajnah M
Am J Med Genet A 2019 Jul;179(7):1338-1345. Epub 2019 May 18 doi: 10.1002/ajmg.a.61168. PMID: 31102500
Pehlivan D, Karaca E, Aydin H, Beck CR, Gambin T, Muzny DM, Bilge Geckinli B, Karaman A, Jhangiani SN; Centers for Mendelian Genomics, Gibbs RA, Lupski JR
Eur J Hum Genet 2014 Sep;22(9):1145-8. Epub 2014 Jan 15 doi: 10.1038/ejhg.2013.291. PMID: 24424126Free PMC Article
Smigiel R, Barg E, Gabrysz M, Szpich E, Sasiadek M, Sasiadek M
Clin Dysmorphol 2012 Jul;21(3):167-169. doi: 10.1097/MCD.0b013e3283541e03. PMID: 22555342
Rufo-Campos M, Riveros-Huckstadt P, RodrIguez-Criado G, Hernández-Soto R
Brain Dev 2004 Apr;26(3):209-12. doi: 10.1016/S0387-7604(03)00133-5. PMID: 15030912
Pascual-Castroviejo I, Santolaya JM, Martin VL, Rodriguez-Costa T, Tendero A, Mulas F
Dev Med Child Neurol 1975 Jun;17(3):343-51. doi: 10.1111/j.1469-8749.1975.tb04673.x. PMID: 1204988

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