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  2. Hammer toe - Wikipedia

    en.wikipedia.org/wiki/Hammer_toe

    Mallet toe is a similar condition affecting the distal interphalangeal joint. [2] Claw toe is another similar condition, with dorsiflexion of the proximal phalanx on the lesser metatarsophalangeal joint, combined with flexion of both the proximal and distal interphalangeal joints. Claw toe can affect the second, third, fourth, or fifth toes.

  3. Van De Berghe Dequeker syndrome - Wikipedia

    en.wikipedia.org/wiki/Van_De_Berghe_Dequeker...

    Van Den Berghe Dequeker syndrome, also known as ulnar hypoplasia-split foot syndrome is a very rare congenital limb malformation syndrome which is characterized by severe ulnar hypoplasia, absence of the index to pinky finger in both hands, and split-foot.

  4. Sclerodactyly - Wikipedia

    en.wikipedia.org/wiki/Sclerodactyly

    Treatment of sclerodactyly is by physical therapy, phototherapy, surgery, topical corticosteroids or vitamin D analogues, and systemic immunosuppressive drugs when the condition is part of systemic scleroderma [citation needed]. Localized treatment won't halt systemic disease, but can restore function and cosmetic aspects of the affected digits.

  5. Charcot–Marie–Tooth disease - Wikipedia

    en.wikipedia.org/wiki/Charcot–Marie–Tooth...

    Charcot–Marie–Tooth disease; Other names: Charcot–Marie–Tooth neuropathy, peroneal muscular atrophy, Dejerine-Sottas syndrome: The foot of a person with Charcot–Marie–Tooth disease: The lack of muscle, a high arch, and claw toes are signs of this genetic disease.

  6. Ectrodactyly - Wikipedia

    en.wikipedia.org/wiki/Ectrodactyly

    Split hand/foot malformation (SHFM) is characterized by underdeveloped or absent central digital rays, clefts of hands and feet, and variable syndactyly of the remaining digits. SHFM is a heterogeneous condition caused by abnormalities at one of multiple loci, including SHFM1 (SHFM1 at 7q21-q22), SHFM2 (Xq26), SHFM3 (FBXW4/DACTYLIN at 10q24 ...

  7. X-linked Charcot–Marie–Tooth disease - Wikipedia

    en.wikipedia.org/wiki/X-linked_Charcot–Marie...

    X-linked Charcot–Marie–Tooth disease type 6: This subtype is characterized by childhood-onset gradual but progressive variable distal muscle weakness and atrophy affecting the lower extremities, distal limb panmodal sensorial anomalies, high-arched feet, claw toes, ankle areflexia, and steppage gait.

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  9. Hereditary motor and sensory neuropathy - Wikipedia

    en.wikipedia.org/wiki/Hereditary_motor_and...

    Symptoms of these disorders include: fatigue, pain, lack of balance, lack of feeling, lack of reflexes, and lack of sight and hearing, which result from muscle atrophy. Patients can also have high arched feet, hammer toes, foot drop, foot deformities, and scoliosis. These symptoms are a result of severe muscular weakness and atrophy.