Kocher Debre Semelaigne Syndrome

We present a 5-year-old boy with poor growth and delayed dental and motor development. Bhide MP Khare MD Jaykar AV Ranade AY Patnekar PN. Kocher Debre Semelaigne disease. Kochers incision used in cholecystectomy. This syndrome is named after the famous Swiss surgeon and Nobel Prize winner Emil Theodor Kocher 1841-1917 and the two French pediatricians Robert Debré 1882-1978 and Georges Sémélaigne born 1892. Kocher-Debré-Sémélaigne syndrome KDSS is a rare association of muscular pseudohypertrophy and hypothyroidism in children. 1 Aunque el síndrome fue reportado inicialmente.

The patient responded well to extract thyroid with improvement of hypothyroidism and diminution in the size of the muscles.

KocherDebreSemelaigne syndrome hypothyroidism in infancy or childhood characterised by lower extremity or generalized muscular hypertrophy myxoedema short stature and cretinism. 2630449 Indexed for MEDLINE Publication Types. Association of muscular pseudohypertrophy and hypothyroidism in children. Em 1892 Kocher citado por Norris e Panner22 descreveu pela primeira vez a ocorrência de alterações mus culares aumento das massas musculares debilidade e lentidão nos movi. Kocher-Debré-Sémélaigne KDSS is a rare presentation of juvenile hypothyroidism manifesting as calf muscle pseudohypertrophy delayed contraction and relaxation of reflexes and percussion myxedema. 3679483 PubMed - indexed for MEDLINE Publication Types.

Facial Features In The Same Girl With Kocher Debre Semelaigne Syndrome Download Scientific Diagram

Kocher debre semelaigne syndrome. 3679483 PubMed - indexed for MEDLINE Publication Types. Kocher-Debre-Semelaigne KDS syndrome is a myopathy of hypothyroidism associated with pseudohypertrophy in infancy or childhood. Em 1892 Kocher citado por Norris e Panner22 descreveu pela primeira vez a ocorrência de alterações mus culares aumento das massas musculares debilidade e lentidão nos movi.

We present a case of Kocher-Debré-Semelaigne syndrome with rhabdomyolysis secondary to Hashimotos thyroiditis. Yeshwanth M Benakappa DG Gautham KS. 2630449 Indexed for MEDLINE Publication Types.

Among the patients with myopathy. FORTES-REGO A deficiencia congênita da glândula tireóide determina um defeito no desenvolvimento corporal e cretinismo 9. The electromyogram was normal.

SÍNDROME DE KOCHER-DEBRÉ-SEMELAIGNE J. Kochers incision used in cholecystectomy. We present a 5-year-old boy with poor growth and delayed dental and motor development.

Association of Kocher-Debré-Semelaigne syndrome-a myopathy of hypothyroidism in childhood characterized by muscular hypertrophy with rhabdomyolysis is very rare. Histologic examination of a muscle did not show changes specific for any disease. Kocher-Debré-Sémélaigne KDSS is a rare presentation of juvenile hypothyroidism manifesting as calf muscle pseudohypertrophy delayed contraction and relaxation of reflexes and percussion myxedema.

It uniquely presents with short stature and delayed bone age unlike other causes of precocious puberty. Kocher-Debré-Sémélaigne syndrome KDSS is a rare association of muscular pseudohypertrophy and hypothyroidism in children. A combination of macroglossia developmental delay stunting and pseudohypertrophy of muscles clinches the diagnosis of KocherDebréSemelaigne syndrome KDS.

There was no family history. We report a case of autoimmune hypothyroidism where weakness and growth failure were predominant complaints and hypertrophied calf muscles were easily noticeable.

Figure 1 Kocher Debre Semelaigne Syndrome Hypothyroid Muscular Pseudohypertrophy A Rare Report Of Two Cases

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Figure 2 Kocher Debre Semelaigne Syndrome Hypothyroid Muscular Pseudohypertrophy A Rare Report Of Two Cases

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1 Aunque el síndrome fue reportado inicialmente.

Association of Kocher-Debré-Semelaigne syndrome-a myopathy of hypothyroidism in childhood characterized by muscular hypertrophy with rhabdomyolysis is very rare. 1 Aunque el síndrome fue reportado inicialmente. Kocher Debre Semelaigne syndrome. He had muscular symptoms. 6862615 PubMed - indexed for MEDLINE Publication Types. Kocher-Debre-Semelaigne KDS syndrome is a myopathy of hypothyroidism associated with pseudohypertrophy in infancy or childhood. Kocher Debre Semelaigne disease. El síndrome de Kocher-Debré-Semelaigne es una enfermedad rara de niños caracterizada por hipotiroidismo moderado o severo de larga duración asociado a una pseudohipertrofia muscular o aumento de la masa muscular por aumento de volumen de los tejidos intersticiales pero con atrofia de células musculares con la subsecuente miotonia. FORTES-REGO A deficiencia congênita da glândula tireóide determina um defeito no desenvolvimento corporal e cretinismo 9.

We present a case of Kocher-Debré-Semelaigne syndrome with rhabdomyolysis secondary to Hashimotos thyroiditis. Association of Kocher-Debré-Semelaigne syndrome-a myopathy of hypothyroidism in childhood characterized by muscular hypertrophy with rhabdomyolysis is very rare. We present a case of Kocher-Debré-Semelaigne syndrome with rhabdomyolysis secondary to Hashimotos thyroiditis. 3679483 PubMed - indexed for MEDLINE Publication Types. We report a case of autoimmune hypothyroidism where weakness and growth failure were predominant complaints and hypertrophied calf muscles were easily noticeable. Kochers incision used in cholecystectomy. 1 Aunque el síndrome fue reportado inicialmente.