
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Turner syndrome physical examination
Introduction
Overview
Overview
Physical examination may be suggestive of thyroid dysfunction, congenital heart defects, inflammatory bowel disease, characteristic skeletal deformities and body habitus/skin manifestations.
Physical Examination
Physical Examination
Appearance of the Patient
- Patient may show signs of poor growth velocity and malnutrition indicative of failure to thrive.
- Patients may be hyperactive.
- The presence of short stature, a webbed neck, pigmented nevi, puffiness of the hands and feet, a cubitus valgus deformity, genu valgum on physical examination are highly suggestive of Turner syndrome.
Vital Signs
- High-grade / low-grade fever
- Hypothermia / hyperthermia may be present
- Tachycardia with regular pulse or irregularly irregular pulse – Hyperthyroidism
- Bradycardia with regular pulse or irregularly irregular pulse – Hypothyroidism
- Tachypnea – Secondary to Acute pulmonary edema from ischemic heart disease
- Hypertension in the upper extremities with hypotension in the lower extremities, decreased post ductal oxygen saturation in the lower extremities, absent lower extremity pulses – Coarctation of aorta
- Widened pulse pressure + water hammer pulse – Aortic Regurgitation secondary to aortic dissection
Skin
- Lymphedema of hands and feet
- Toe nail cellulitis
- Vitiligo
- Alopecia
- Nail hypoplasia
- Psoriasis – silver scaled erythrematous plaques present on extensor surfaces
- Pigmented melanocytic nevi – avoid rubbing against clothes.
- Hyperconvex nails
- Oslers nodes, Jane way lesions]] – Infective Endocarditis
HEENT
Ear
- Weber test may be abnormal- Conductive hearing loss or sensorineural hearing loss
- Rinne test may be positive – Conductive hearing loss or sensorineural hearing loss
- External ear canal deformities may be noted.
Eye
- Prominent epicanthal folds
- Bilateral epicanthus
- Strabismus
- Ptosis
- Cataract
- Nystagmus
- Roth spots – secondary to infective endocarditis
Neck
- Pterygium colli
- Low posterior hair line
- Loose skin on the nape of newborns
- Jugular venous distension – Rule out Eisenmengirsation secondary to congenital heart defects, pressure may be transmitted to the internal jugular vein.
- Hepatojugular reflux – There is an increased risk of ischemic heart disease and cardiomyopathy secondary to this may cause Right sided heart failure.
Lungs
- Pulmonary examination of patients with Turner syndrome is usually normal.
- Fine/coarse crackles upon auscultation of the lung bases/apices unilaterally/bilaterally (rule out)
Heart
- Patient has a wide shield shaped chest with inverted nipples.
- S3 (rule out)
- S4 (rule out)
- Gallops (rule out)
- A pansystolic murmur heard over the tricuspid area – Ventricular Septal defect
- Early blowing diastolic murmur head over the left upper sternal border – Aortic regurgitation secondary to aortic dissection
- Systolic ejection click followed by a crescendo decrescendo murmur (early P2 and delayed A2) – Early onset aortic stenosis secondary to a bicuspid aortic valve
- Fever + Petechiae + Heart murmur – Infective Endocarditis
Abdomen
- Look for signs of inflammatory bowel disease such as fistulas, skin tags and oral aphtous ulcers
Back
Genitourinary
- Chronic estrogen deficiency may lead to signs of atrophic vaginitis
- Rudimentary uterus
- Palpable mass secondary to dysgerminoma or gonadoblastoma
Neuromuscular
- Neuromuscular examination of patients with Turner syndrome is usually normal.
Extremities
- Shortened limbs
- Shortened 4th metacarpal
- Cubitus valgus deformity
- Madelung deformity
- Cyanosis – Secondary to structural heart defects
- Pitting edema of the upper/lower extremities – Hypothyroidism
- Muscle atrophy
References
References
- ↑ Bucerzan S, Miclea D, Popp R, Alkhzouz C, Lazea C, Pop IV; et al. (2017). “Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)”. Ther Clin Risk Manag. 13: 613–622. doi:10.2147/TCRM.S126301. PMC 5422538. PMID 28496331.
- ↑ 2.0 2.1 Vaddadi S, Murthy RS, Rahul CH, Kumar VL (2013). “A rare case of Turner’s syndrome presenting with Mullerian agenesis”. J Hum Reprod Sci. 6 (4): 277–9. doi:10.4103/0974-1208.126313. PMC 3963314. PMID 24672170.
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Akash Daswaney, M.B.B.S[2]
