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Hypoplasia of the nasal bone
- ... in lateral meningocele syndrome include a high and nasal voice, hearing loss, abnormalities of the heart or the genitourinary system, poor ...
- ... skin (hyperpigmentation), typically on the chest and back; abnormalities of the teeth; and a broad nasal bridge with a rounded tip of the nose. ...
- ... inward and upward turning foot (club foot), and abnormalities of the long bones of the arms and legs. CHARGE syndrome occurs ...
- Paget's Disease of Bone: Diagnosis and Treatment (Mayo Foundation for Medical Education and Research)Paget's Disease of Bone/Diagnosis and Tests ... Paget's Disease of Bone ... Mayo Foundation for Medical Education and Research
- What Are Common Symptoms of Klinefelter Syndrome (KS)?
(Eunice Kennedy Shriver National Institute of Child Health and Human Development)
Klinefelter Syndrome/Learn More ... Klinefelter Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes ... - ... continues to cover and protect the ends of bones and is present in the nose and external ears. Type XI collagen is also ... people with fibrochondrogenesis type 1, a disorder of bone growth characterized by severe skeletal abnormalities, hearing loss, and vision loss. Infants with fibrochondrogenesis ...
- ... continues to cover and protect the ends of bones and is present in the nose and external ears. Type XI collagen is also ...
- ... continues to cover and protect the ends of bones and is present in the nose, airways, and external ears.The RUNX2 protein is a transcription factor, which means it attaches (binds) to specific regions ... cells that build bones (osteoblasts) and in the development of teeth.The ...
- ... for diarrhea and dislocated joints, LI for limb abnormalities and little size, and NO for slender nose and normal intelligence.The varied signs and symptoms ...
- ... continues to cover and protect the ends of bones and is present in the nose and external ears.Cartilage cells use sulfate ions ... and in early childhood, SLC26A2 gene mutations prevent bones from developing ... skeletal abnormalities seen in achondrogenesis type 1B. More About This ...