Craniosynostosis Autosomal Dominant
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Craniosynostosis Autosomal Dominant Overview

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Learn About Craniosynostosis Autosomal Dominant

What is the definition of Craniosynostosis Autosomal Dominant?
Craniosynostosis that is autosomal dominant is a genetic condition (inherited from a parent) in which the bones of the skull in an infant close too early. In newborns, the skull is made up of plates of bone that have flexible joints called sutures that close as infants grow. Craniosynostosis occurs when the sutures of the skull close prematurely, which causes pressure to build up inside the head, along with a misshapen skull.
What are the symptoms of Craniosynostosis Autosomal Dominant?
Symptoms of craniosynostosis that is autosomal dominant may include asymmetry (unevenness) of the head and face, a bulging soft spot on the top of head (fontanelle), an enlarged head, lethargy, bulging scalp veins, irritability, high-pitched cry, poor feeding, projectile vomiting, and delayed development.
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What are the current treatments for Craniosynostosis Autosomal Dominant?
Treatment for craniosynostosis that is autosomal dominant depends on which skull sutures are involved. Craniosynostosis usually requires surgery unless the condition is very mild. Some infants may be able to wear special helmets designed to reshape the skull, and some may need evaluation for developmental and learning delays. Parents who carry the autosomal dominant gene for craniosynostosis should consider genetic counseling.
Who are the top Craniosynostosis Autosomal Dominant Local Doctors?
Experienced in Craniosynostosis Autosomal Dominant
Dr. Erica Fernandes
Medical Genetics | Pediatrics
Experienced in Craniosynostosis Autosomal Dominant
Dr. Erica Fernandes
Medical Genetics | Pediatrics
26901 76th Avenue, 
New Hyde Park, NY 
718-470-3265
Languages Spoken:
English

Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Hyde Park, New York. Dr. Fernandes is rated as an Experienced provider by MediFind in the treatment of Craniosynostosis Autosomal Dominant. She is also highly rated in 153 other conditions, according to our data. Her clinical expertise encompasses Microcephaly, Chromosome 13q Deletion, Hennekam Syndrome, and Acrodermatitis Enteropathica.

Experienced in Craniosynostosis Autosomal Dominant
Dr. Julie Kaplan
Pediatrics
Experienced in Craniosynostosis Autosomal Dominant
Dr. Julie Kaplan
Pediatrics

Cleveland Clinic Main Campus

10524 Euclid Avenue, 
Cleveland, OH 
216-444-2200
Experience:
29+ years
Languages Spoken:
English
See accepted insurances

Julie Kaplan is a Pediatrics provider practicing medicine in Cleveland, Ohio. She has been practicing medicine for over 29 years. Dr. Kaplan is rated as an Experienced provider by MediFind in the treatment of Craniosynostosis Autosomal Dominant. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Mosaicism, Gingival Fibromatosis with Hypertrichosis, Mixed Gonadal Dysgenesis, and Turner Syndrome. Dr. Kaplan is board certified in American Board Of Medical Genetics And Genomics, 2020.

 
 
 
 
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Experienced in Craniosynostosis Autosomal Dominant
Dr. Raymond Y. Wang
Medical Genetics
Experienced in Craniosynostosis Autosomal Dominant
Dr. Raymond Y. Wang
Medical Genetics
1201 West La Veta Avenue, 
Orange, CA 
888-770-2462
Languages Spoken:
English
See accepted insurances

Raymond Wang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Wang is rated as an Experienced provider by MediFind in the treatment of Craniosynostosis Autosomal Dominant. He is also highly rated in 50 other conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.

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