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Rh of October the Cretan Assembly once more voted the union with Greece, and in the absence of M. Zaimis—who had gone for a holiday to Santa Maura—elected a committee of six to govern the island in the name of the king of Greece.

Against this the Mussulman deputies protested, in a memorandum addressed to the British secretary of state for foreign affairs. His reply, while stating that his government would safeguard the interests of the Mussulmans, left open the question of the attitude of the powers, complicated now by sympathy with reformed Turkey. The efforts of diplomacy were directed to allaying the resentment of the “Young Turks” on the one hand and the ardour of the Greek unionists on the other; and meanwhile the Cretan administration was carried on peaceably in the name of King George. At last (July 13, 1909) the powers announced to the Porte, in answer to a formal remonstrance, their decision to withdraw their remaining troops from Crete by July 26 and to station four war-ships off the island to protect the Moslems and to safeguard “the supreme rights” of the Ottoman Empire. This arrangement, which was duly carried out, was avowedly “provisional” and satisfied neither party, leading in Greece especially to the military and constitutional crises of 1909 and 1910.

—Pashley, Travels in Crete (2 vols., Cambridge and London, 1837); Spratt, Travels and Researches in Crete (2 vols., London, 1867); Raulin, Description physique de l’île de Crète (3 vols, and Atlas, Paris, 1869); W. J. Stillman, The Cretan Insurrection of 1866–68 (New York, 1874); Edwardes, Letters from Crete (London, 1887); Stavrakis,  (Athens, 1890); J. H. Freese, A Short Popular History of Crete (London, 1897); Bickford-Smith, Cretan Sketches (London, 1897); Laroche, La Crète ancienne et moderne (Paris, 1898); Victor Berard, Les Affaires de Crète (Paris, 1898); Monumenti Veneti dell’ isola de Creta (published by the Venetian Institute), vol. i. (1906), vol. ii. (1908). See also Mrs Walker, Eastern Life and Scenery (London, 1886), and Old Tracks and New Landmarks (London, 1897); H. F. Tozer, The Islands of the Aegean (Oxford, 1890); J. D. Bourchier, “The Stronghold of the Sphakiotes,” Fortnightly Review (August 1890); E. J. Dillon, “Crete and the Cretans,” Fortnightly Review (May 1897).

 CRETINISM, the term given to a chronic disease, either sporadic or endemic, arising in early childhood, and due to absence or deficiency of the normal secretion of the thyroid gland. It is characterized by imperfect development both of mind and body. The thyroid gland is either congenitally absent, imperfectly developed, or there is definite goitre. The origin of the word is doubtful. Its southern French form Chrestiaa suggested to Michel a derivation from cresta (crête), the goose foot of red cloth worn by the Cagots of the Pyrenees. The Cagots, however, were not cretins. The word is usually explained as derived from chrétien (Christian) in the sense of “innocent.” But Christianus (which appears in the Lombard cristanei; compare the Savoyard innocents and gens du bon dieu) is probably a translation of the older cretin, and the latter is probably connected with creta (craie)—a sallow or yellow-earthy complexion being a common mark of cretinism.

The endemic form of cretinism prevails in certain districts, as in the valleys of central Switzerland, Tirol and the Pyrenees. In the United Kingdom cretins have been found in England at Oldham, Sholver Moor, Crompton, Duffield, Cromford (near Matlock), and other points in Derbyshire; endemic goitre has been seen near Nottingham, Chesterfield, Pontefract, Ripon, and the mountainous parts of Staffordshire and Yorkshire, the east of Cumberland, certain parts of Worcester, Warwick, Cheshire, Monmouth, and Leicester, near Horsham in Hampshire, near Haslemere in Surrey, and near Beaconsfield in Buckingham. There are cretins at Chiselborough in Somerset. In Scotland cretins and cases of goitre have been seen in Perthshire, on the east coast of Fife, in Roxburgh, the upper portions of Peebles and Selkirk, near Lanark and Dumfries, in the east of Ayrshire, in the west of Berwick, the east of Wigtown, and in Kirkcudbright. The disease is not confined to Europe, but occurs in North and South America, Australia, Africa and Asia. Wherever endemic goitre is present, endemic cretinism is present also, and it has been constantly observed that when a new family moves into a goitrous district, goitre appears in the first generation, cretinism in the second. The causation of goitre has now been shown to be due to drinking certain waters, though the particular impurity in the water which gives rise to this condition has not been determined (see ). The causation of the sporadic form of cretinism is, however, obscure.

Cretinism usually remains unrecognized until the child reaches some eighteen months or two years, when its lack of mental development and uncouth bodily form begin to attract attention. Occasionally the child appears to be normal in infancy, but the cretinoid condition develops later, any time up to puberty. The essential point in the morbid anatomy of these cases is the absence or abnormal condition of the thyroid gland (see ). It may be congenitally absent, atrophied, or the seat of a goitre, though this last condition is very rare in cases of sporadic cretinism. The skeleton shows arrested growth, most marked in the case of the long bones. The skull in the endemic form of cretinism is usually brachycephalic, but in the sporadic cases it is more commonly dolichocephalic. The pathology of cretinism and its allied condition (q.v.) has now been conclusively worked out, and its essential cause has been shown to be loss of function of the thyroid gland.

The condition has existed and been described in far back ages, but mingled with so many other entirely different deformities and degenerations that it is now often almost impossible to classify them satisfactorily. The following is a vivid picture by Beaupré (Dissertation sur les crétins, translated in Blackie on Cretinism, Edin., 1855):—

“I see a head of unusual form and size, a squat and bloated figure, a stupid look, bleared hollow and heavy eyes, thick projecting eyelids, and a flat nose. His face is of a leaden hue, his skin dirty, flabby, covered with tetters, and his thick tongue hangs down over his moist livid lips. His mouth, always open and full of saliva, shows teeth going to decay. His chest is narrow, his back curved, his breath asthmatic, his limbs short, misshapen, without power. The knees are thick and inclined inward, the feet flat. The large head drops listlessly on the breast; the abdomen is like a bag.”

When fully grown the height rarely exceeds 4 ft., and is often less than 3 ft. The skin feels doughy from thickening of the subcutaneous tissues, and it hangs in folds over the abdomen and the bends of the joints. Very frequently there is an umbilical hernia. The hair has a far greater resemblance to horse-hair than to that of a human being, and is usually absent on the body of an adult cretin. The temperature is subnormal, and the exposed parts tend to become blue in cold weather. The blood is usually deficient in haemoglobin, which is often only 40-50% of the normal. The mental capacity varies within narrow limits; an intelligent adult cretin may reach the intellectual development of a child 3-4 years of age, though more often the standard attained is even below this. The child cretin learns neither to walk nor talk at the usual time. Often it is unable even to sit without support. Some years later a certain power of movement is acquired, but the gait is waddling and clumsy. Speech is long delayed, or in bad cases may be almost entirely lacking. The voice is usually harsh and unpleasant. Of the senses smell and taste are but slightly developed, more or less deafness is generally present, and only the sight is fairly normal. In the adult the genital organs remain undeveloped. If the cretin is untreated he rarely has a long life, thirty years being an exceptional age. Death results from some intercurrent disease.

Cretinism has to be distinguished from the state of a Mongolian idiot, in whom there is no thickening of the subcutaneous tissues, and much greater alertness of mind; from achondroplasia, in which condition there is usually no mental impairment; and from infantilism, which covers a group of symptoms whose only common point is that the primary and secondary sexual characteristics fail to appear at the proper time.

Before 1891 there was no treatment for this disease. The patients lived in hopeless imbecility until their death. But in that year Dr George Murray published his discovery of the effect of hypodermic injections of thyroid gland extract in cases of myxoedema. In the following year Drs Hector Mackenzie, E. L. Fox of Plymouth, and Howitz of Copenhagen, each working independently, showed the equally potent effect of the gland administered by the mouth. The remedy was soon