Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 24 for Muenke syndrome
Did you mean menkes syndrome?
  1. Muenke syndrome 
    Muenke syndrome is a condition characterized by the premature closure of certain bones of the skull (craniosynostosis) during ... individuals have an enlarged head (macrocephaly). People with Muenke syndrome may also have mild abnormalities of the hands ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
  2. FGFR3 gene 
    ... the FGFR3 gene has been shown to cause Muenke syndrome, which is a condition that causes craniosynostosis and ... abnormalities, and developmental delays. The variant that causes Muenke syndrome substitutes the amino acid arginine for the amino ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  3. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics
  4. Saethre-Chotzen syndrome 
    ... by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome. Eur J Hum Genet. 2006 Jan;14(1): ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
  5. TWIST1 gene 
    ... by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome. Eur J Hum Genet. 2006 Jan;14(1): ...
    https://medlineplus.gov/genetics/gene/twist1 - Genetics
  6. Opitz G/BBB syndrome 
    ... 285. Citation on PubMed Robin NH, Opitz JM, Muenke M. Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
  7. Prader-Willi syndrome 
    ... 2022 Jan 30. Citation on PubMed Wattendorf DJ, Muenke M. Prader-Willi syndrome. Am Fam Physician. 2005 Sep 1;72(5): ...
    https://medlineplus.gov/genetics/condition/prader-willi-syndrome - Genetics
  8. SADDAN 
    ... 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans. Endocr Rev. 2000 Feb;21( ...
    https://medlineplus.gov/genetics/condition/saddan - Genetics
  9. Crouzon syndrome with acanthosis nigricans 
    ... 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans. Endocr Rev. 2000 Feb;21( ...
    https://medlineplus.gov/...rouzon-syndrome-with-acanthosis-nigricans - Genetics
  10. Hypochondroplasia 
    ... 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans. Endocr Rev. 2000 Feb;21( ...
    https://medlineplus.gov/genetics/condition/hypochondroplasia - Genetics
previous · 1 · 2 · 3 · next