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 42 for Miller syndrome
  1. Miller syndrome 
    Miller syndrome is a rare condition that mainly affects the development of the face and limbs. The severity ... this disorder varies among affected individuals.Children with Miller syndrome are born with underdeveloped cheek bones (malar hypoplasia) ...
    https://medlineplus.gov/genetics/condition/miller-syndrome - Genetics
  2. Miller-Dieker syndrome 
    Miller-Dieker syndrome is a condition characterized by a pattern of abnormal brain development called lissencephaly. Normally, the surface ... with fewer folds and grooves. In people with Miller-Dieker syndrome, lissencephaly is typically associated with severe intellectual disabilities, ...
    https://medlineplus.gov/genetics/condition/miller-dieker-syndrome - Genetics
  3. Guillain-Barré syndrome 
    ... and can have abnormal or absent reflexes (areflexia).Miller Fisher syndrome, another type of Guillain-Barré syndrome, involves cranial ... to various areas of the head and neck. Miller Fisher syndrome is characterized by three features: weakness or paralysis ...
    https://medlineplus.gov/genetics/condition/guillain-barre-syndrome - Genetics
  4. Alagille syndrome 
    ... Hepatofacioneurocardiovertebral syndrome Paucity of interlobular bile ducts Watson-Miller syndrome Genetic Testing Registry: Alagille syndrome due to a ...
    https://medlineplus.gov/genetics/condition/alagille-syndrome - Genetics
  5. 17 alpha-hydroxylase/17,20-lyase deficiency 
    ... j.fertnstert.2013.11.011. Citation on PubMed Miller WL. The syndrome of 17,20 lyase deficiency. J Clin Endocrinol ...
    https://medlineplus.gov/...-alpha-hydroxylase-17-20-lyase-deficiency - Genetics
  6. Prader-Willi syndrome 
    ... article on PubMed Central Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Prader-Willi syndrome. Genet Med. 2012 Jan;14(1):10-26. ... 2007 May 23. Citation on PubMed Driscoll DJ, Miller JL, Cassidy SB. Prader-Willi Syndrome. 1998 Oct 6 [updated 2024 Dec 5]. In: ...
    https://medlineplus.gov/genetics/condition/prader-willi-syndrome - Genetics
  7. Apert syndrome 
    ... No abstract available. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  8. Crouzon syndrome 
    ... 2004.12.037. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics
  9. Beare-Stevenson cutis gyrata syndrome 
    ... 2002.610309.x. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/.../beare-stevenson-cutis-gyrata-syndrome - Genetics
  10. Crouzon syndrome with acanthosis nigricans 
    ... 21.1.0387. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/...rouzon-syndrome-with-acanthosis-nigricans - Genetics
previous · 1 · 2 · 3 · 4 · 5 · next