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Results 11 - 20 of 189 for Hypoplasia of the nasal bone
  1. Trichorhinophalangeal syndrome type II 
    ... joint malformations; distinctive facial features; intellectual disability; and ... bone tumors called osteochondromas. Affected individuals may develop a ...
    https://medlineplus.gov/.../trichorhinophalangeal-syndrome-type-ii - Genetics
  2. Crouzon syndrome with acanthosis nigricans 
    ... fluid in the brain (hydrocephalus) can also occur. Nasal passage abnormalities and hydrocephalus are rare in Crouzon syndrome. Less common features of Crouzon syndrome with acanthosis nigricans include subtle changes in the bones of the spine (vertebrae), abnormalities of the finger ...
    https://medlineplus.gov/...rouzon-syndrome-with-acanthosis-nigricans - Genetics
  3. Trichorhinophalangeal syndrome type I 
    ... bone and joint malformations; distinctive facial features; and abnormalities of the ... of one or more bones in the fingers or toes are abnormally cone- ...
    https://medlineplus.gov/.../trichorhinophalangeal-syndrome-type-i - Genetics
  4. Alpha-mannosidosis 
    ... rounded eyebrows, large ears, flattened bridge of the nose, protruding jaw, widely spaced teeth, overgrown gums, and large tongue. The skeletal abnormalities that can occur in this disorder include reduced bone density (osteopenia), thickening of the bones at the ...
    https://medlineplus.gov/genetics/condition/alpha-mannosidosis - Genetics
  5. Apert syndrome 
    ... of Apert syndrome. Premature fusion of the skull bones prevents the head from growing normally, which leads to a sunken appearance in the middle of the face (midface hypoplasia), a beaked nose, a wrinkled forehead, and an opening in the ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  6. Simpson-Golabi-Behmel syndrome 
    ... gene have distinctive facial features including an upturned nose, a wide mouth, and a prominent chin. Their fingernails may be malformed and they can have extra nipples. Skeletal abnormalities, including extra spinal bones (vertebrae), are also possible in affected females. Other ...
    https://medlineplus.gov/.../condition/simpson-golabi-behmel-syndrome - Genetics
  7. KBG syndrome 
    ... prominent nasal bridge, a long space between the nose and upper lip (long philtrum), and a thin upper lip.A common skeletal abnormality in people with KBG syndrome is slowed mineralization of bones (delayed bone age); for example, an affected 3- ...
    https://medlineplus.gov/genetics/condition/kbg-syndrome - Genetics
  8. Atelosteogenesis type 1 
    ... cases absent. As a result of the limb bone abnormalities, individuals with this condition have very short arms and legs. Characteristic facial features include a prominent forehead, wide-set eyes (hypertelorism), an upturned nose with a grooved tip, and a very small ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-1 - Genetics
  9. Renal tubular dysgenesis 
    ... including the lungs. Oligohydramnios causes a set of abnormalities called the Potter ... In addition, bone development in the skull is abnormal in some ...
    https://medlineplus.gov/genetics/condition/renal-tubular-dysgenesis - Genetics
  10. Ear Disorders (National Library of Medicine)  
    Your ear has three main parts: outer, middle and inner. You use all of them in hearing. Sound waves come in through your outer ear. They reach your middle ...
    https://medlineplus.gov/eardisorders.html - Health Topics
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