Haim–Munk syndrome

Haim–Munk syndrome (pronounced: hahy-m muhngk) is a rare autosomal recessive disorder characterized by palmoplantar keratoderma, severe early onset periodontitis, onychogryphosis, pes planus, arachnodactyly, and acro-osteolysis. It was first described by Haim and Munk in 1965.

Etymology

The syndrome is named after Dr. S. Haim and Dr. M. Munk, who first described the condition in 1965.

Symptoms

The primary symptoms of Haim–Munk syndrome include:

• Palmoplantar keratoderma: Thickening of the skin on the palms of the hands and soles of the feet.
• Periodontitis: Severe inflammation of the gums that can lead to tooth loss.
• Onychogryphosis: Abnormal thickening and curvature of the nails.
• Pes planus: Flat feet.
• Arachnodactyly: Abnormally long and slender fingers and toes.
• Acro-osteolysis: Absorption of the distal phalanges of the hands and feet.

Diagnosis

Diagnosis of Haim–Munk syndrome is typically based on the presence of the characteristic clinical features. Genetic testing can confirm the diagnosis.

Treatment

Treatment for Haim–Munk syndrome is symptomatic and supportive. This may include skin care for the palmoplantar keratoderma, dental care for the periodontitis, and orthopedic interventions for the pes planus and acro-osteolysis.

See also

• List of cutaneous conditions
• List of dental abnormalities associated with cutaneous conditions

External links

• Medical encyclopedia article on Haim–Munk syndrome
• Wikipedia's article - Haim–Munk syndrome

This WikiMD dictionary article is a stub. You can help make it a full article.

---

Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski