Craniosynostosis-fibular aplasia syndrome
| Craniosynostosis-fibular aplasia syndrome | |
|---|---|
| Other names | Craniosynostosis with fibular aplasia Lowry syndrome |
Craniosynostosis-fibular aplasia syndrome (also known as craniosynostosis with fibular aplasia or Lowry syndrome) is a rare syndrome characterized by bicoronal craniosynostosis, absent fibula, cryptorchidism, and bilateral simian creases.[1][2][3]
Signs and symptoms[edit]
Features of this condition include:[1]
- Limbs: fibular aplasia, single transverse palmar crease
- Genitourinary system: cryptorchidism
- Musculoskeletal system: craniosynostosis
History[edit]
The first (and only) reported cases of this syndrome were two brothers first described in 1972. Both had normal intelligence. A follow-up report was made on one the brothers in 1993 at age 25 with two years of college education.[1][2]
Causes[edit]
This condition is genetic but little is known of its cause. Autosomal recessive inheritance has been suggested.[1][2]
References[edit]
- ^ a b c d "Craniosynostosis-fibular aplasia syndrome (Concept Id: C1857492)". www.ncbi.nlm.nih.gov. Retrieved 2023-09-14.
- ^ a b c "218550 - CRANIOSYNOSTOSIS WITH FIBULAR APLASIA". www.omim.org. Retrieved 2023-09-14.
- ^ "Resources: Craniosynostosis-fibular aplasia syndrome". Rare Disease InfoHub. Retrieved September 14, 2023.