Craniosynostosis Maroteaux Fonfria type
Overview
Craniosynostosis Maroteaux Fonfria type: A rare disorder which is similar to a condition called Apert syndrome but also involves extra fingers and toes. Apert syndrome is characterized by abnormalities in the appearance of the face and head as well as finger and toe abnormalities. The bones of the skull fuse together too early which prevents it from growing normally.
Symptoms
The list of signs and symptoms mentioned in various sources for Craniosynostosis Maroteaux Fonfria type includes the 28 symptoms listed below: * Extra little finger * Extra big toe * Partially or totally joined fingers * Partially or totally joined toes * Premature joining of bones in the head * Growth disturbance in the skull * Long-shaped head * Wide set eyes * Bulging eyes * Narrow roof of mouth * Bone abnormalities of the jaw * Sunken appearance in middle of face * Beaked nose * Underdeveloped jaw * Crowded teeth * Beaked nose * Shallow eye socket * Visual disturbances * Hearing loss * Cleft palate * Severe acne * Intellectual impairment * Progressive hydrocephalus * Hippocampal abnormalities * Megalencephaly * Flat face * Delayed teeth eruption * Maloclusion
Causes
* Beaked nose * Beaked nose * Bulging eyes * Cleft palate * Crowded teeth * Delayed teeth eruption * Flat face * Hearing loss * Intellectual impairment * Severe acne * Visual disturbances * Wide set eyes
Diagnosis
The phrase "signs of Craniosynostosis Maroteaux Fonfria type" should, strictly speaking, refer only to those signs and symptoms of Craniosynostosis Maroteaux Fonfria type that are not readily apparent to the patient. The word "symptoms of Craniosynostosis Maroteaux Fonfria type" is the more general meaning; see symptoms of Craniosynostosis Maroteaux Fonfria type. The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Craniosynostosis Maroteaux Fonfria type. This medical information about signs and symptoms for Craniosynostosis Maroteaux Fonfria type has been gathered from various sources, may not be fully accurate, and may not be the full list of Craniosynostosis Maroteaux Fonfria type signs or Craniosynostosis Maroteaux Fonfria type symptoms. Furthermore, signs and symptoms of Craniosynostosis Maroteaux Fonfria type may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Craniosynostosis Maroteaux Fonfria type symptoms.