Adducted thumb syndrome - Misplaced Pages

(Redirected from Adducted thumb syndrome recessive form) Rare genetic disease affecting palate, thumbs, and upper limbs Medical condition

Adducted thumb syndrome
Other names	Christian syndrome, craniostenosis arthrogryposis cleft palate

Adducted thumb syndrome has a lysosomal recessive pattern of inheritance
Causes	mutation in the CHST14 gene

Adducted thumb syndrome recessive form is a rare disease affecting multiple systems causing malformations of the palate, thumbs, and upper limbs. The name Christian syndrome derives from Joe. C. Christian, the first person to describe the condition. Inheritance is believed to be autosomal recessive, caused by mutation in the CHST14 (carbohydrate sulfotransferase 14) gene.

Signs and symptoms

This syndrome is characterised by typical facial appearance, slight build, thin and translucent skin, severely adducted thumbs, arachnodactyly, club feet, joint instability, facial clefting and bleeding disorders, as well as heart, kidney or intestinal defects. Severe psychomotor and developmental delay and decreased muscle tone may also be present during infancy. Cognitive development during childhood is normal.

Cause

This section is empty. You can help by adding to it. (April 2017)

Diagnosis

The syndrome is associated with microcephaly, arthrogryposis and cleft palate and various craniofacial, respiratory, neurological and limb abnormalities, including bone and joint defects of the upper limbs, adducted thumbs, camptodactyly and talipes equinovarus or calcaneovalgus. It is characterized by craniosynostosis, and myopathy in association with congenital generalized hypertrichosis. Patients with the disease are considered intellectually disabled. Most die in childhood. Patients often have respiratory difficulties such as pneumonia, and from seizures due to dysmyelination in the brain's white matter. It has been hypothesized that the Moro reflex (startle reflex in infants) may be a tool in detecting the congenital clasped thumb early in infancy. The thumb normally extends as a result of this reflex.

Treatment

This section is empty. You can help by adding to it. (April 2017)

References

Fitch N, Levy EP (1975). "Adducted thumb syndromes". Clin. Genet. 8 (3): 190–8. doi:10.1111/j.1399-0004.1975.tb01493.x. PMID 1175322. S2CID 31187237.
"CHST14". National Center for Biotechnology Information database. NCBI. Retrieved 21 March 2013.
"Ehlers-Danlos syndrome, musculocontractural type – Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". Archived from the original on 2019-12-13. Retrieved 2013-04-01.
Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 1008. ISBN 978-1-4160-2999-1.
Kunze J, Park W, Hansen KH, Hanefeld F (1983). "Adducted thumb syndrome. Report of a new case and a diagnostic approach". Eur. J. Pediatr. 141 (2): 122–6. doi:10.1007/BF00496805. PMID 6662143. S2CID 13243887.
Anderson TE, Breed AL (1981). "Congenital clasped thumb and the Moro reflex. (Letter)". The Journal of Pediatrics. 99: 664–665. doi:10.1016/s0022-3476(81)80293-4.

External links

Whonamedit.com entry on Christian syndrome

Classification	D OMIM: 201550 DiseasesDB: 31689

v t e Congenital abnormality syndromes
Craniofacial	Acrocephalosyndactyly Apert syndrome Carpenter syndrome Pfeiffer syndrome Saethre–Chotzen syndrome Sakati–Nyhan–Tisdale syndrome Bonnet–Dechaume–Blanc syndrome Other Baller–Gerold syndrome Cyclopia Goldenhar syndrome Moebius syndrome Pierre Robin sequence
Short stature	1q21.1 deletion syndrome Aarskog–Scott syndrome Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome Robinow syndrome Silver–Russell syndrome Seckel syndrome Smith–Lemli–Opitz syndrome Snyder–Robinson syndrome Turner syndrome
Limbs	Adducted thumb syndrome Holt–Oram syndrome Klippel–Trénaunay syndrome Nail–patella syndrome Rubinstein–Taybi syndrome Gastrulation/mesoderm: Caudal regression syndrome Ectromelia Sirenomelia VACTERL association
Overgrowth syndromes	Bannayan–Riley–Ruvalcaba syndrome Beckwith–Wiedemann syndrome Benign symmetric lipomatosis Klippel–Trénaunay syndrome Neurofibromatosis type I Perlman syndrome Proteus syndrome Sotos syndrome Tatton-Brown–Rahman syndrome Weaver syndrome
Laurence–Moon–Bardet–Biedl	Bardet–Biedl syndrome Laurence–Moon syndrome
Combined/other, known locus	2 (Feingold syndrome) 3 (Zimmermann–Laband syndrome) 4/13 (Fraser syndrome) 8 (Branchio-oto-renal syndrome, CHARGE syndrome) 12 (Keutel syndrome, Timothy syndrome) 15 (Marfan syndrome) 19 (Donohue syndrome) Multiple Fryns syndrome

Categories: