Zur Dyscephalie mit Catarakta congenita und Hypotrichose

Weyers, H

doi:10.1007/bf00438720

Cited by 16 publications

(5 citation statements)

References 11 publications

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“…An occipital protrusion was seen by Bergmeister (1911) and Ludwig and Körting (1950), and frontal protrusion prominence of the frontal bosses), by Schondel (1943, Case 3), Marchesani (1949), Ullrich and Fremerey-Dohna (1953), Leffertstra (1956), and Gregersen (1956). Bulging of the parietal bones was mentioned by Bergmeister (1911), Schondel (1943, Case 4), Ludwig andKörting (1950), Ullrich and Fremerey-Dohna (1953), and Weyers (1954). In some cases the forehead was narrow, elevated, and receding (Streiff, 1950;Ludwig and Körting, 1950;Leff ertstra, 1956).…”

Section: Symptomatologymentioning

confidence: 96%

“…(3) Nanism.-Body height is not given, Case 13 (Weyers, 1954; Figs. 14 and 15).-A boy aged 16 years showed the fol¬ lowing symptoms :…”

Section: Negative Signsmentioning

confidence: 99%

“…In some cases the forehead was narrow, elevated, and receding (Streiff, 1950;Ludwig and Körting, 1950;Leff ertstra, 1956). There may be aplasia of the malar bone (Ludwig and Körting, 1950;Weyers, 1954).…”

Section: Symptomatologymentioning

confidence: 99%

“…1911;Biodi, 1957; personal observation). Open bite is not uncommon (Ludwig and Kört¬ ing, 1950; personal observation), nor is hiatodontia (Weyers, 1954). Open bite is not uncommon (Ludwig and Kört¬ ing, 1950; personal observation), nor is hiatodontia (Weyers, 1954).…”

Section: Symptomatologymentioning

confidence: 99%

“…Cases 20 and 21). Lashes are short, thin, scanty, and sometimes also lacking (Schondel, 1943, Case 3;Moehlig, 1946;Weyers, 1954).…”

Section: Symptomatologymentioning

confidence: 99%

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A New Syndrome

François¹

1958

AMA Arch Ophthalmol

120

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Section: Symptomatologymentioning

confidence: 96%

“…(3) Nanism.-Body height is not given, Case 13 (Weyers, 1954; Figs. 14 and 15).-A boy aged 16 years showed the fol¬ lowing symptoms :…”

Section: Negative Signsmentioning

confidence: 99%

Section: Symptomatologymentioning

confidence: 99%

Section: Symptomatologymentioning

confidence: 99%

“…Cases 20 and 21). Lashes are short, thin, scanty, and sometimes also lacking (Schondel, 1943, Case 3;Moehlig, 1946;Weyers, 1954).…”

Section: Symptomatologymentioning

confidence: 99%

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A New Syndrome

François¹

1958

AMA Arch Ophthalmol

120

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Hallermann-Streiff Syndrome

Steele¹,

Bass²

1970

Am J Dis Child

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A patient with the Hallermann-Streiff syndrome showed significant findings, including demonstration of decreased thoracic compliance and a marked response of growth hormone to arginine stimulation. (Fig 1 to 3). The cranial sutures including the metopic and squamosal were widely separated, and the fontanelles were large. Frontal and occipital bossing and craniotabes were noted. Skin over the scalp was atrophie, and there was hypotrichosis of the scalp, eyelashes, and eye¬ brows (Fig 1 and 2). There was striking microphthalmia with a corneal diameter of 7 mm, and the eyes also appeared proptotic; sclerae were blue and funduscopy was normal. The nose was thin and beak¬ like with marked cutaneous atrophy (Fig 1 to 3) Roentgenograms of the skull showed absence of the angle of the mandible, widely separated sutures, large fonta¬ nelles, extremely thin cortex of the skull, and wormian bones in the parietal areas bilaterally (Fig 4). Skeletal survey re¬ vealed hypoplastic ribs and clavicles, par¬ ticularly at the acromial ends (Fig 5). There was shortening of the first metacarpal bilaterally. The cardiothoracic ratio was 0.65, and the cardiac configuration was unusual (Fig 5).At 8

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Syndrome

Schmid

1973

Pädiatrische Radiologie

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Zur Dyscephalie mit Catarakta congenita und Hypotrichose

Cited by 16 publications

References 11 publications

A New Syndrome

A New Syndrome

Hallermann-Streiff Syndrome

Syndrome

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